| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs3672445 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Gmcl1 | GRCm38.p3 | 6:86735321 | CAGTCCCCTGCCCTC[A/G]TCCCCTGCCCTGACT | 23885 |
| rs6374125 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Gmcl1 | Mm_Celera | 6:86715961 | CATTTTCCAGACCTG[C/T]CATAGATGTCTTGGT | 23885 |
| rs6374655 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Gmcl1 | Mm_Celera | 6:86716053 | CTCAGCTGTGTATCA[C/T]CAACACTCCAGGACA | 23885 |
| rs6375229 | snp | A/G | 0.5 | 0 | intron-variant | Gmcl1 | Mm_Celera | 6:86716168 | AGGGTAAGAGGAGTG[A/G]GGGTGgagtgagaga | 23885 |
| rs29832921 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Gmcl1 | Mm_Celera | 6:86709941 | GCAGATGTATTTGAT[C/G]GAACATGTTTAAGAA | 23885 |
| rs29871475 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86697545 | GCGCAATCTAGAATT[A/T]AAAAAAAAAATACAA | 23885 |
| rs29876329 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86693190 | AGCTGCACCCATCCA[G/T]CCAGCCCATTAGCTG | 23885 |
| rs30017664 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86694926 | GCCATCCTTGTTCCC[A/G]AACACCTCACCAGGC | 23885 |
| rs30110426 | snp | C/T | 0.304688 | 0.243945 | downstream-variant-500B | Gmcl1 | GRCm38.p3 | 6:86691509 | TAGTCGTAACAGAAT[C/T]CTGCTTTAAAAGAAA | 23885 |
| rs30119583 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86714969 | AATGAAGCTTTTTTT[A/T]AAAAGATTTATTTAT | 23885 |
| rs30158247 | snp | C/G | 0.432133 | 0.171253 | upstream-variant-2KB | Gmcl1 | GRCm38.p3 | 6:86733756 | AGCCTCCAGGTCTTG[C/G]CTTCCTTCTGCTGCC | 23885 |
| rs30160860 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86696885 | ACAGGATAGAAAAAG[C/T]CCTCACAGCTCTGTA | 23885 |
| rs30169438 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86700130 | CCATTCAACTACTTG[C/T]TCCTATCAATGCAGA | 23885 |
| rs30215270 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Gmcl1 | GRCm38.p3 | 6:86733623 | CCCTGTACGGTTAAT[A/G]AGAGGACGGACTTGC | 23885 |
| rs30217735 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86698221 | GGCAGCAAGGCTTCA[C/T]GTGTCTCTCCCCCCA | 23885 |
| rs30262805 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86705064 | TTCGGCCTCATAGGC[A/G]CTGGGATCACACGTC | 23885 |
| rs30269247 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86695027 | GACAGCCAGGACCAC[A/G]GAGTGAGACACTGGC | 23885 |
| rs30322189 | snp | A/C | 0.498615 | 0.0262793 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86710090 | CACTGGTTAACCAAC[A/C]TGACAATACCCAGAG | 23885 |
| rs30364969 | snp | A/G | 0.32 | 0.24 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86723698 | AGCAGAGACAGCCAG[A/G]CCTCAGTTGAATTGG | 23885 |
| rs30371897 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86714968 | CAATGAAGCTTTTTT[A/T]TAAAAGATTTATTTA | 23885 |
| rs30409954 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86694921 | CACTTGCCATCCTTG[C/T]TCCCGAACACCTCAC | 23885 |
| rs30413416 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86695347 | ATGCACTTGATCCGC[A/G]GAACTAGAGCTGCAG | 23885 |
| rs30419259 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Gmcl1 | GRCm38.p3 | 6:86700517 | GCCATCCTACCTAAA[C/T]GCTATGCTCCTTCGA | 23885 |
| rs30419872 | snp | A/T | 0.48 | 0.0979796 | upstream-variant-2KB | Gmcl1 | GRCm38.p3 | 6:86734448 | TTCTCCTCTCCTAAA[A/T]CTATACTTTGAATGG | 23885 |
| rs30458085 | snp | G/T | 0.375 | 0.216506 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86714347 | AATTTTATATGTGTG[G/T]ATGAGAGAGAGAGAG | 23885 |
| rs30460609 | snp | A/T | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86728583 | CAGAATTTAAAAAAA[A/T]ATATATTCATATGCT | 23885 |
| rs30520083 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86709607 | CAGGGCCTGCACTCA[A/G]ATACATAAAGACACA | 23885 |
| rs30562133 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gmcl1 | Mm_Celera | 6:86724843 | ATCTTTCTTAAAAAC[C/T]TTTAGGCTAAATTCG | 23885 |
| rs30562224 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86721904 | GACCACCTCTGTGCC[C/T]ATTCACACCCGGTCT | 23885 |
| rs30608133 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86729676 | AAACTGCGACTACGT[A/G]TCCACTTACATTCAT | 23885 |
| rs30660917 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gmcl1 | Mm_Celera | 6:86724849 | CTTAAAAACCTTTAG[A/G]CTAAATTCGTCAAGT | 23885 |
| rs30661315 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86713820 | TGATAGTGGAGAGAT[A/G]TACCAGGGGCCACCT | 23885 |
| rs30669294 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gmcl1 | Mm_Celera | 6:86697079 | TAAAGTCTAAACATA[A/G]ATTCATTTGTATTTT | 23885 |
| rs30702912 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gmcl1 | Mm_Celera | 6:86715588 | GGCTGCTCAATCTAT[C/T]TCTTTTTCTTTCCCT | 23885 |
| rs30759501 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gmcl1 | Mm_Celera | 6:86723414 | TTAGTTTAAATTTTT[A/T]AAATTTTACTTTTAA | 23885 |
| rs30759998 | snp | A/C | 0.375 | 0.216506 | downstream-variant-500B | Gmcl1 | GRCm38.p3 | 6:86691710 | ATCTTGAAAAAACCC[A/C]AAAACTAAAAAAAAC | 23885 |
| rs30804890 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86696111 | ATGCCATAGCCTCTC[A/G]TACTGGGCGACACTA | 23885 |
| rs30902500 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86726609 | CTGCAGCAAACTGTT[A/G]CTCAATTATAATCCA | 23885 |
| rs30902954 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86726325 | TACACCATTAAGTCT[C/T]GTTTTTGCCCTGTTA | 23885 |
| rs30903463 | snp | A/T | 0.375 | 0.216506 | intron-variant | Gmcl1 | Mm_Celera | 6:86729497 | AAATTAAAGAAATAG[A/T]GGCCATAAATTTGAA | 23885 |
| rs30905729 | snp | A/G | 0.375 | 0.216506 | intron-variant | Gmcl1 | Mm_Celera | 6:86723313 | TTTCATATAAAAAAC[A/G]TAATAATTAAAATAG | 23885 |
| rs30907206 | snp | A/T | 0.49827 | 0.0293608 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86695558 | GCCATGAGAAAATAC[A/T]CATACTGCCAGGAGT | 23885 |
| rs30907473 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gmcl1 | Mm_Celera | 6:86697937 | TTCATGCCTTTAATC[C/T]TAGCACTTGGGAGCA | 23885 |
| rs30953428 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gmcl1 | Mm_Celera | 6:86723179 | GTAGTTTTATATGAC[C/T]ACAGAGGATTCTGAA | 23885 |
| rs30959821 | snp | C/G | 0.32 | 0.24 | missense | Gmcl1 | Mm_Celera | 6:86692940 | AGTGTCCTGGGTTTT[C/G]TGGGTGACGATTACT | 23885 |
| rs36248057 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86700763 | TTCAAATTCTCAAGT[C/G]ATCTTCTGTCACTGC | 23885 |
| rs36253787 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86708495 | AATGTTCCCAGGGCT[A/G]AGGTCAACTAATGAG | 23885 |
| rs36260216 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Gmcl1 | Mm_Celera | 6:86718472 | TTCAACAGGACTTGT[C/T]TTTTCCTGTTCTTAC | 23885 |
| rs36263577 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86711426 | GCTGTAAAAGGCTGT[A/C]AAAGGCTGAGGTAGG | 23885 |
| rs36268176 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Gmcl1 | Mm_Celera | 6:86712985 | CTTGACCACCAAAAT[A/G]CTACGATGGAAGGTT | 23885 |
| rs36278437 | snp | C/T | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86693491 | GAGTCACTGCTGTCA[C/T]CACCACCACAGCTCC | 23885 |
| rs36291647 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime | Gmcl1 | GRCm38.p3 | 6:86692708 | TACCTACAGCAATTT[C/T]TACTGCTACTAAATT | 23885 |
| rs36295791 | snp | A/G | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86703807 | TTTGAAAGTCAAAGT[A/G]GAGGTAAATTTGGGA | 23885 |
| rs36306333 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Gmcl1 | Mm_Celera | 6:86716809 | ATTTATAACAAAGAG[A/G]TAAGTGCCGAGCTTA | 23885 |
| rs36313448 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86694657 | ATGGTGAAGTGCCCC[C/T]TGCTGGTCTACAATG | 23885 |
| rs36335154 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Gmcl1 | Mm_Celera | 6:86722651 | ACCACTGAACATACT[A/G]GAAAAGTAGCCAGAC | 23885 |
| rs36359321 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86708225 | AGGTCTTACTGGTTT[C/G]GACTTTACCCAATGG | 23885 |
| rs36369666 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86694613 | CAAAGCTTTTACACC[A/G]TACCATATGCCTCCA | 23885 |
| rs36387585 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86697118 | ATTCATACAGACAGA[C/T]TCAAGGTAATTTTTG | 23885 |
| rs36387913 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gmcl1 | Mm_Celera | 6:86693659 | GATCTCACAGATTTG[C/T]CACCAGGACTACAGA | 23885 |
| rs36398100 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86698151 | TGGCAATGGTATCAC[C/T]ACGCCCATCCTCAGA | 23885 |
| rs36414824 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86714691 | CTTAACTTTGACATG[A/G]GGTTGTGAGGGATCT | 23885 |
| rs36431088 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86720455 | TCTTCCATCCTCTGT[C/T]CCTGGTCAGAAATGC | 23885 |
| rs36433368 | snp | A/G | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86708728 | GTTAAATAAATGCAC[A/G]GAGGGCACAGAAGAC | 23885 |
| rs36445409 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86701927 | TAGCAAGGGGATCCA[C/T]GAGAGCATGTAGACA | 23885 |
| rs36446320 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86702017 | TTTTTAGAAGTAGCA[C/T]CCAATGAAGCAGGAA | 23885 |
| rs36460641 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Gmcl1 | Mm_Celera | 6:86735264 | TCACTGTTGCTACAA[A/G]CAGGGATGATGGAGA | 23885 |
| rs36471309 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86704985 | AGTTTGGTGTCACCT[C/T]CCCCATACAAGGAAG | 23885 |
| rs36479526 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86705257 | ATCATGAAACTGAAG[A/G]TACGATACAGAATGA | 23885 |
| rs36506007 | snp | C/T | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86709362 | TTAATACAGTTTTGC[C/T]TTCCAGAGACACAAA | 23885 |
| rs36511761 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86706942 | GCTCTGCCTGGAAAG[C/T]TTCCTGTGGGCCAGG | 23885 |
| rs36512164 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Gmcl1 | GRCm38.p3 | 6:86692494 | ACAAGACTTCACCAG[A/G]TGGCTGAACAAATGA | 23885 |
| rs36541525 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gmcl1 | Mm_Celera | 6:86697380 | AAACACACATAAGAC[A/G]CAGTACAGTGGCAAG | 23885 |
| rs36555469 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Gmcl1 | Mm_Celera | 6:86692883 | CCTTGGACGTGAACG[C/T]AGTAGGTCATTAAGT | 23885 |
| rs36560474 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Gmcl1 | Mm_Celera | 6:86712861 | CATCAGAGCAGCTAC[A/G]AGGACAGACAGAACG | 23885 |
| rs36563016 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Gmcl1 | Mm_Celera | 6:86711243 | CTGCATCTACTTCCC[A/G]GTTAGTGATGCACAG | 23885 |
| rs36571716 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Gmcl1 | Mm_Celera | 6:86716694 | CTATCGCCTTTGAAG[C/G]TCTATGCTTGCAGAA | 23885 |
| rs36599175 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Gmcl1 | GRCm38.p3 | 6:86692400 | AAACAAAACCAACTC[C/T]TAAGCTTAATCTCCC | 23885 |
| rs36614918 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86706178 | TAAATAACTGACTCA[C/T]TTTCTGTTTCTTTAT | 23885 |
| rs36623700 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86698324 | GCTGCCCTTCAGTGA[C/T]GCACTTAACTCACTT | 23885 |
| rs36627431 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Gmcl1 | Mm_Celera | 6:86710372 | AGAGTATTCACATGC[C/T]CATCTCTTGGGCATA | 23885 |
| rs36663187 | snp | A/G | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86699627 | CTTTTAGCTGGGACT[A/G]TCTAATTAGCCTGAA | 23885 |
| rs36685180 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Gmcl1 | Mm_Celera | 6:86708121 | TATTAAGTTCTCTGT[C/G]ACAACACTTCATTCT | 23885 |
| rs36685577 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86715957 | TCTTCATTTTCCAGA[C/T]CTGTCATAGATGTCT | 23885 |
| rs36721166 | snp | A/G | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86701951 | GTAGACAGGGGCTAC[A/G]AGCTGAAGCCCAGGC | 23885 |
| rs36726083 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86696112 | TGCCATAGCCTCTCG[C/T]ACTGGGCGACACTAA | 23885 |
| rs36728021 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Gmcl1 | Mm_Celera | 6:86714118 | ACCACAGAAGCAATG[C/T]GAAGTAATATTCTTT | 23885 |
| rs36733257 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Gmcl1 | GRCm38.p3 | 6:86717927 | CTTTATTACATTCTC[A/G]TAAGACTCCAAAACA | 23885 |
| rs36736022 | snp | A/C | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Gmcl1 | Mm_Celera | 6:86704214 | TACTGAGCAGCACGG[A/C]TCTAACCCGTGTTCA | 23885 |
| rs36746421 | snp | A/T | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86694453 | CAGTTAAATCTGGCC[A/T]CGGGTAGATCAAAGA | 23885 |
| rs36748370 | snp | C/T | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86704779 | CACACTCAGCACTGA[C/T]AAAGGAAAAAGAATA | 23885 |
| rs36748907 | snp | A/C | 0.42 | 0.183303 | intron-variant | Gmcl1 | Mm_Celera | 6:86695556 | TGGCCATGAGAAAAT[A/C]CACATACTGCCAGGA | 23885 |
| rs36749970 | snp | A/T | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86709447 | AAATTTTATATCCTT[A/T]AAGATGGGGCTGGGG | 23885 |
| rs36757282 | snp | A/C/T | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86709742 | GATGTTTACCACACA[A/C/T]TAAAACTACTATAGG | 23885 |
| rs36768224 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Gmcl1 | Mm_Celera | 6:86713786 | GGGTTGGTGGAATGA[A/C]TTAGCATTATCAGTA | 23885 |
| rs36774335 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gmcl1 | Mm_Celera | 6:86712772 | CTCCCTTGCAGGCTA[C/T]AAAAGGATGTGTATG | 23885 |
| rs36819311 | snp | C/T | 0.32 | 0.24 | intron-variant | Gmcl1 | Mm_Celera | 6:86721513 | GAAGCAGAAAGGACA[C/T]TAGTCTGCACCTGGA | 23885 |
| rs36830554 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Gmcl1 | Mm_Celera | 6:86721644 | TGTCTAATCTTGACA[C/T]AGTCAGTGGTTAGAA | 23885 |
| rs36860303 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Gmcl1 | Mm_Celera | 6:86704651 | CTGAGTTTAAAAGAA[C/T]GGAAAGTTTTTCTAC | 23885 |
| rs36874120 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Gmcl1 | Mm_Celera | 6:86707447 | CATAGCCAGCCACTG[C/T]TGTTTATACACTGCC | 23885 |