| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs3655000 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Chfr, Gm15787 | Mm_Celera | 5:110168670 | CTGACACCTTTTCAA[A/G]CACATACACAGTATA | 231600 |
| rs3671914 | snp | C/T | 0.456747 | 0.140554 | synonymous-codon, intron-variant | Chfr, Gm15787 | Mm_Celera | 5:110169179 | CTGCTACTGGGGCCG[C/T]AACTGTCGCACTCAG | 231600 |
| rs3673880 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chfr | Mm_Celera | 5:110153501 | CTTGAAGGACTCTTA[C/T]TTCAATTTTAATTAA | 231600 |
| rs3726156 | snp | A/G | 0.42 | 0.183303 | intron-variant, nc-transcript-variant | Chfr, Gm15787 | Mm_Celera | 5:110168243 | CCAGGTAAGGAGCCC[A/G]CGAACCATTTCTGTC | 231600 |
| rs6342764 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Chfr | Mm_Celera | 5:110158085 | AGGTAGCATTCCAGT[A/G]CTTCCTGCCTGAGGC | 231600 |
| rs13473079 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Chfr, Gm15787 | Mm_Celera | 5:110170963 | AATGTTTTTTAAAAG[A/G]CCCCATACAAACACT | 231600 |
| rs29513246 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chfr | Mm_Celera | 5:110142903 | CAGGAGCCACACCAC[C/T]GTCAGTGGAAAACCC | 231600 |
| rs29531817 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Chfr | Mm_Celera | 5:110147292 | GACCTCTGCACGTGT[A/G]CCAAGGCACACTCGA | 231600 |
| rs29550291 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chfr | Mm_Celera | 5:110152514 | CGCTAACTTTTCTGT[C/T]GTAGGGACCTGGGGC | 231600 |
| rs29566526 | snp | C/T | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Chfr | Mm_Celera | 5:110164432 | TGAGTACACTGTCAC[C/T]GTCCTCAGACACACT | 231600 |
| rs29580239 | snp | C/T | 0.375 | 0.216506 | intron-variant | Chfr | Mm_Celera | 5:110145325 | TGGTCTTATGACTGA[C/T]TCCTTCATGTATCAT | 231600 |
| rs29581541 | snp | A/G | 0.5 | 0 | intron-variant | Chfr | Mm_Celera | 5:110139135 | ACAGTGGCAATTTTG[A/G]AATTTTTGATTCTTT | 231600 |
| rs29630757 | snp | C/G | 0.5 | 0 | intron-variant | Chfr | Mm_Celera | 5:110141107 | TTTCTGTGAGTTTGT[C/G]TGAAGGCCTTGTTTT | 231600 |
| rs29635003 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Chfr | Mm_Celera | 5:110137641 | ACACTAAAAGTTTTA[C/T]GGGATTTTAAATGGA | 231600 |
| rs29635507 | snp | C/T | 0.375 | 0.216506 | intron-variant | Chfr | Mm_Celera | 5:110154281 | TAAATTGGGTGTGGC[C/T]GCTGACCCCTTTCAT | 231600 |
| rs29636420 | snp | A/C | 0.5 | 0 | intron-variant | Chfr | Mm_Celera | 5:110156483 | CATACCATGTGTATT[A/C]TTTTGTGATTGCATT | 231600 |
| rs29681871 | snp | A/G | 0.32 | 0.24 | intron-variant | Chfr | Mm_Celera | 5:110161751 | CAGCTACTGTAGCAA[A/G]AAGCTTCTCTGAAGA | 231600 |
| rs29682606 | snp | C/T | 0.33241 | 0.236027 | intron-variant, nc-transcript-variant | Chfr, Gm15787 | Mm_Celera | 5:110168013 | TCCAAATGTCTAACC[C/T]ATTGAGTTGATGTGT | 231600 |
| rs29774191 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Chfr | Mm_Celera | 5:110165701 | CGAGGCCTTTGCAGA[C/G]AGACCCTGTCTCATA | 231600 |
| rs29779536 | snp | A/T | 0.475309 | 0.108333 | utr-variant-3-prime, intron-variant | Chfr, Gm15787 | Mm_Celera | 5:110171260 | CCTTGTACCTTGACT[A/T]TGGTTAAAATGGGAA | 231600 |
| rs29779825 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chfr | Mm_Celera | 5:110142798 | CGGGAGAATCTTTCC[C/T]GTCCCCACACTCTGG | 231600 |
| rs33040078 | snp | C/T | 0.375 | 0.216506 | intron-variant | Chfr | Mm_Celera | 5:110154153 | AGTTCAAAGCTAGCC[C/T]GAGAAGCATAGGCAC | 231600 |
| rs33042508 | snp | G/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Chfr, Gm15787 | Mm_Celera | 5:110167424 | TCAAACCCACATAAT[G/T]GTTTACAGCTATCCA | 231600 |
| rs33048228 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Chfr | Mm_Celera | 5:110143352 | TGATTTGTTATAAGT[A/G]GGTAGTGACAGGCAA | 231600 |
| rs33099011 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Chfr | Mm_Celera | 5:110142622 | AATTATTGTGCAAGC[C/T]TGAAATACAAATTCC | 231600 |
| rs33103576 | snp | C/G | 0.375 | 0.216506 | intron-variant | Chfr | Mm_Celera | 5:110143811 | GGTTCTTGGTGTAAG[C/G]ACTTGGGTGGAGTGC | 231600 |
| rs33132600 | snp | C/T | 0.32 | 0.24 | intron-variant | Chfr | Mm_Celera | 5:110162455 | CTCCTCTTTCCCCGA[C/T]CAGTGCTAGTGTTGC | 231600 |
| rs33139082 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Chfr | Mm_Celera | 5:110141574 | TGGCACAAGCAATAG[A/G]TAGCCTGGCAGTACA | 231600 |
| rs33155306 | snp | C/T | 0.375 | 0.216506 | intron-variant | Chfr | Mm_Celera | 5:110142025 | GCCCAGCTTTTTTAA[C/T]TCTTAACACTGTAAA | 231600 |
| rs33283675 | snp | G/T | 0.498615 | 0.0262793 | intron-variant | Chfr | Mm_Celera | 5:110158343 | GCTCAGCAACTGGAG[G/T]TAGATACTTGACCAC | 231600 |
| rs33319514 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Chfr | Mm_Celera | 5:110152140 | TACTATTTTTTTATT[A/T]TGTGTCTTCTAACAC | 231600 |
| rs33346354 | snp | A/T | 0.444444 | 0.157135 | upstream-variant-2KB | Chfr | Mm_Celera | 5:110134551 | GGGAATTGACATCCT[A/T]CTTGGCAGAAAGAAA | 231600 |
| rs33355971 | snp | C/T | 0.375 | 0.216506 | intron-variant | Chfr | Mm_Celera | 5:110154827 | ATAGCTCTGCTTCTT[C/T]TCCTCGCAGTCAGCC | 231600 |
| rs33386024 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Chfr | Mm_Celera | 5:110147969 | AATGGCTTGGTGGTT[A/C]AGAGCCTTTACTCTT | 231600 |
| rs33453166 | snp | C/T | 0.5 | 0 | intron-variant | Chfr | Mm_Celera | 5:110165027 | GAGGGAGTCAGATCT[C/T]GTTACGGATGGTTGT | 231600 |
| rs33472256 | snp | C/T | 0 | 0 | intron-variant | Chfr, Gm15787 | Mm_Celera | 5:110170200 | ACCTCCAAACAGACA[C/T]ATACCTACCACTAAA | 231600 |
| rs33519464 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Chfr | Mm_Celera | 5:110135048 | GCCACTGCTACTTTT[A/G]TATCCTTTCAAAAGT | 231600 |
| rs33526998 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Chfr | Mm_Celera | 5:110148496 | GTGGCTCACGACCAT[C/T]TGTAATGTGATCCCA | 231600 |
| rs33560342 | snp | C/T | 0.375 | 0.216506 | intron-variant | Chfr | Mm_Celera | 5:110150977 | TTCACCTGCCTCTGC[C/T]TTCTGAGTGCTAGGA | 231600 |
| rs33566448 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Chfr, Gm15787 | Mm_Celera | 5:110170367 | GGAGAGGGGAGAGTG[A/G]CCTCCGTTACCTCAG | 231600 |
| rs33659930 | snp | A/G | 0.5 | 0 | intron-variant | Chfr | Mm_Celera | 5:110150049 | CTGGAGATAGTGTTA[A/G]AGGTGGTTATGAGCT | 231600 |
| rs33669734 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Chfr | Mm_Celera | 5:110163134 | GAATTGTAATATGTT[C/T]AGTTCTGCACCCTCT | 231600 |
| rs33715399 | snp | C/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Chfr, Gm15787 | Mm_Celera | 5:110167766 | ATTTAAAATTTTAAT[C/G]CACGGGTGATTATTT | 231600 |
| rs33724097 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Chfr | Mm_Celera | 5:110160782 | GTTCTCTATTTAAGA[C/T]TGCATTTTAGTTTGA | 231600 |
| rs33755132 | snp | A/G | 0.5 | 0 | intron-variant | Chfr | Mm_Celera | 5:110138593 | GGCAGAGAAGAACTG[A/G]TGAGTAGCTGACACT | 231600 |
| rs33755657 | snp | C/G | 0.375 | 0.216506 | intron-variant | Chfr | Mm_Celera | 5:110145314 | CATACAGTATGTGGT[C/G]TTATGACTGACTCCT | 231600 |
| rs45633572 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Chfr | Mm_Celera | 5:110143103 | CCTCAGGGTCCACCT[G/T]GAGGCATGCCAGAAA | 231600 |
| rs45687440 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110146730 | TTTTTGCAGAAGAAC[A/G]TGGATCTGCCTCAGG | 231600 |
| rs45745021 | snp | A/G | 0.345679 | 0.230967 | upstream-variant-2KB | Chfr | Mm_Celera | 5:110134818 | CAGTTCCCAAATGTG[A/G]ACAGTGGCCCAGCCA | 231600 |
| rs45832496 | snp | C/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Chfr, Gm15787 | Mm_Celera | 5:110168269 | CTGTCTGTATTGGTG[C/T]CACCACTCAGTTCTA | 231600 |
| rs45849345 | snp | C/T | | | intron-variant | Chfr | Mm_Celera | 5:110137733 | TTTTTTCTTTTTTGG[C/T]TTTTTGAGGCAAGGT | 231600 |
| rs45878825 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110158183 | GATAGCCTTAGGAGC[C/T]CTGCCCCTTAGCTGT | 231600 |
| rs45878843 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110166721 | TCTTTGAATGCCTCT[G/T]TGTGAGTGTTAACAA | 231600 |
| rs45888249 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110153330 | GGGATAAGAAGTACG[C/T]TAGTGCTGTGCTTCA | 231600 |
| rs45898764 | snp | A/C | 0.18 | 0.24 | intron-variant | Chfr | Mm_Celera | 5:110138791 | GAGTCCACTTTAGAG[A/C]CCAGTTATAGAGCCC | 231600 |
| rs45946428 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110165175 | AATAGGAGTAGCTCA[A/T]ACAGAAAGTATGAGT | 231600 |
| rs46063487 | snp | C/G | 0.124444 | 0.216185 | downstream-variant-500B, intron-variant | Chfr, Gm15787 | Mm_Celera | 5:110172276 | TTAACCCCTGGCCCT[C/G]TACGCAGGTCCACAG | 231600 |
| rs46064955 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Chfr | Mm_Celera | 5:110144064 | CCTGAAATACTTGAA[A/G]ACCACCATAAAGTTA | 231600 |
| rs46157409 | snp | C/G | 0.165289 | 0.235211 | upstream-variant-2KB | Chfr | Mm_Celera | 5:110135326 | GTTTCTCTCTCACCG[C/G]GGGGTCACCAACATG | 231600 |
| rs46194243 | snp | C/T | 0.132653 | 0.220748 | missense | Chfr | Mm_Celera | 5:110146502 | ATCTCCCCAAAAGGA[C/T]GCAGTTCACTTGTTG | 231600 |
| rs46198170 | snp | A/G | 0.345679 | 0.230967 | utr-variant-5-prime, upstream-variant-2KB | Chfr | Mm_Celera | 5:110135902 | GGTGGCGGCGACTGT[A/G]AGGCCGGTTCCGGGA | 231600 |
| rs46222624 | snp | A/T | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Chfr, Gm15787 | Mm_Celera | 5:110170327 | GCCACTTTCTGCATC[A/T]TCTCCAATGTTGCTC | 231600 |
| rs46276298 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110159452 | GCATCCTGGGATAGG[C/T]AGCTAACAAGTCCCA | 231600 |
| rs46284669 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110159305 | GCACAGTGTCTGATA[C/T]AGTACAAGCTCTCCA | 231600 |
| rs46366481 | snp | G/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Chfr | Mm_Celera | 5:110136013 | GTGCTGAGCGTTTTT[G/T]AAGTAGTCCCTGAGC | 231600 |
| rs46396852 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Chfr | Mm_Celera | 5:110166991 | AAATGTACAAGTCAT[G/T]TCTTGTATGTGATTT | 231600 |
| rs46493949 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110163254 | CTACTTTTATGTACA[C/T]TAAAAGACCTTTCAG | 231600 |
| rs46518318 | snp | C/T | 0.18 | 0.24 | upstream-variant-2KB | Chfr | Mm_Celera | 5:110134723 | TGATTGGTGGAATAA[C/T]TTAGCACAGATGTTT | 231600 |
| rs46528444 | snp | A/C/G | 0.152778 | 0.230321 | intron-variant | Chfr | GRCm38.p3 | 5:110142790 | AGTTCTTTCGGGAGA[A/C/G]TCTTTCCTGTCCCCA | 231600 |
| rs46598440 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Chfr | Mm_Celera | 5:110142674 | GAATGAGGCTGCAGC[A/G]CCAAGCTTGGTCCAG | 231600 |
| rs46670140 | snp | C/G | 0.197531 | 0.244432 | missense, utr-variant-5-prime, upstream-variant-2KB | Chfr | Mm_Celera | 5:110136077 | ATGGAGCTACACGGG[C/G]AAGAGCAGCCGCCGC | 231600 |
| rs46687398 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110142601 | TGCTATTCCTTGACC[C/G]GAGAGAATTATTGTG | 231600 |
| rs46755110 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Chfr | Mm_Celera | 5:110164661 | GGGAAGGATGGGAGC[A/G]TGGCTAAGGGAGCCT | 231600 |
| rs46766130 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Chfr | Mm_Celera | 5:110138388 | CAGACCCTGTGTCTA[A/C]GTCTGAAAACCAGTA | 231600 |
| rs46769198 | snp | C/T | | | intron-variant, nc-transcript-variant | Chfr, Gm15787 | Mm_Celera | 5:110167612 | AATACCAGTGACCTA[C/T]ATGTTCTAGATAAGG | 231600 |
| rs46892132 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Chfr, Gm15787 | Mm_Celera | 5:110169329 | TGATTTGGGAACTTT[A/C]GGTATACTTCAGTAG | 231600 |
| rs46892732 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Chfr | Mm_Celera | 5:110142844 | TGCGGTTCCCCATCT[A/C]GCAGTGTGATTATAA | 231600 |
| rs46900010 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110163156 | GCACCCTCTGCACTC[A/C]TGTTGAGTACTTTGC | 231600 |
| rs46980830 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110163290 | GCCTTGAACTGTGTC[A/G]GGAAAAATGAAGGCC | 231600 |
| rs47037940 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110158089 | AGCATTCCAGTGCTT[A/C]CTGCCTGAGGCTGGC | 231600 |
| rs47131021 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110141594 | CTGGCAGTACACTGA[A/G]TTGTACACCAACTGG | 231600 |
| rs47169178 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110160295 | TGTGTGTTCTCTTAG[C/T]AAATTTGGGGCCGGT | 231600 |
| rs47242005 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Chfr | Mm_Celera | 5:110146651 | TTAGACTCTACTGTT[C/G]TGTGTATCCTTTGGC | 231600 |
| rs47265557 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Chfr | Mm_Celera | 5:110164177 | ATGAAGTGGTAAGAA[C/T]GTGGCAGGCCACACT | 231600 |
| rs47274846 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Chfr, Gm15787 | Mm_Celera | 5:110168173 | CTGCTGTGGTCTGCG[C/T]AGCTTCCGAGAGCTG | 231600 |
| rs47360752 | snp | A/G | 0.18 | 0.24 | intron-variant | Chfr | Mm_Celera | 5:110138354 | GGTGATGTCTGAATC[A/G]GTGTTTGATGTATCA | 231600 |
| rs47396945 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Chfr, Gm15787 | Mm_Celera | 5:110167156 | TAAATCACCTTCAGG[C/T]AATATGTGTGAGATG | 231600 |
| rs47434775 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110166571 | CTGTGGTATGCACAG[C/T]TGAGTCTGCCTTGTG | 231600 |
| rs47461353 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Chfr | Mm_Celera | 5:110144236 | CATTTTCCCCTTTGG[C/T]TGCTTCCGTATACTT | 231600 |
| rs47482736 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime, intron-variant | Chfr, Gm15787 | Mm_Celera | 5:110171630 | CGACCCAGGGCTGGC[C/T]GAGCCCTTAGCCCTC | 231600 |
| rs47497904 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110162871 | GGACACACGTTTTCT[C/T]TAGCATTTGCCTGCA | 231600 |
| rs47516804 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110153921 | CATGTAATTCCTATA[C/G]TTAGACACTGCGAGT | 231600 |
| rs47544834 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Chfr | Mm_Celera | 5:110142297 | GGTCAGGTCAGGAGA[A/T]AAGCAGAAATCATAG | 231600 |
| rs47574955 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110160071 | TTTCAAAGAGAGTTG[C/T]GCTCTTGAGTCTGGT | 231600 |
| rs47576894 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Chfr | Mm_Celera | 5:110142424 | TTGTGTCAAGATTGA[A/C]GTCTGCATGCTGTTT | 231600 |
| rs47589938 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110161281 | TTAATCCTCTCTGTG[C/T]GTCAAGAAACAAAAC | 231600 |
| rs47606515 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110146366 | CGTGCATCATTCTTA[A/G]GCTGAGATTTCTGAT | 231600 |
| rs47619148 | snp | C/T | 0.18 | 0.24 | upstream-variant-2KB | Chfr | Mm_Celera | 5:110134831 | TGAACAGTGGCCCAG[C/T]CAATCACATTAGAGA | 231600 |
| rs47626548 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Chfr | Mm_Celera | 5:110158068 | AGGGTTGAACTGGCT[A/G]CAGGTAGCATTCCAG | 231600 |
| rs47671403 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Chfr | Mm_Celera | 5:110166921 | ACTGTAGCATTACTA[C/T]TTCACAGTTTATGTT | 231600 |