| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs6181048 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80606532 | CACTTCAGTCACTCA[A/C]CCAACCTTCTGCCAC | 17444 |
| rs6182282 | snp | A/C | 0.5 | 0 | intron-variant | Grap2 | Mm_Celera | 15:80606795 | CAAAGCTGTGAGCCC[A/C]CACCCTGAACCCTTG | 17444 |
| rs6182750 | snp | A/T | 0.5 | 0 | intron-variant | Grap2 | Mm_Celera | 15:80606871 | CTTTCTTAGGCTCCA[A/T]GCTCAANAAAATTGC | 17444 |
| rs6182754 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Grap2 | Mm_Celera | 15:80606878 | AGGCTCCANGCTCAA[A/C]AAAATTGCCTGGCAG | 17444 |
| rs31576971 | snp | C/T | 0.375 | 0.216506 | intron-variant | Grap2 | Mm_Celera | 15:80574724 | CTCTGTGAGTTCAGT[C/T]CCTGGGACTCACATG | 17444 |
| rs31609112 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Grap2 | Mm_Celera | 15:80597717 | AGTTGCCTGTGTCTA[A/G]CCTGGGGTTTCCGAT | 17444 |
| rs31610448 | snp | A/G | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80636280 | TGAAGTCACTTGTCC[A/G]CTCTGCTCACCACTA | 17444 |
| rs31617734 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Grap2 | Mm_Celera | 15:80579301 | ATGAAGTATCCCTCC[A/G]GGAACAGATGGTAAA | 17444 |
| rs31617736 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Grap2 | Mm_Celera | 15:80579562 | TTTCTTATCCCTCAC[A/G]GGCAGTTCAGAAGGC | 17444 |
| rs31617738 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80580109 | GACCTGAGACTAAGG[A/G]ATGGCGTAGTGATTC | 17444 |
| rs31617740 | snp | G/T | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80580187 | ACTGCCTGCATTTGT[G/T]ATTTGCCATTAATGA | 17444 |
| rs31617742 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Grap2 | Mm_Celera | 15:80580534 | GAAGTTAACACTACA[C/T]CCTACACTGAGTGTG | 17444 |
| rs31617744 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Grap2 | Mm_Celera | 15:80598730 | TCCACACAGTTGTGT[A/G]CCGTGGCGGAACCGG | 17444 |
| rs31617746 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Grap2 | Mm_Celera | 15:80598738 | GTTGTGTACCGTGGC[A/G]GAACCGGCTTCCATA | 17444 |
| rs31617748 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Grap2 | Mm_Celera | 15:80598751 | GCGGAACCGGCTTCC[A/G]TAAGCGCCATTGGAT | 17444 |
| rs31617750 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80598783 | CGTAAAGAAATGCTA[C/T]TTTACTTTATTGATT | 17444 |
| rs31617752 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80599017 | TTGATCTGTGAAATA[A/G]CTCATTCCTGGGCGG | 17444 |
| rs31618574 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80599041 | TGGGCGGGCTTGAAG[C/T]TCCCCAGAAACACAG | 17444 |
| rs31618576 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80599116 | ATTACTCCAAAACGG[C/T]TGCACCCAGCCACCC | 17444 |
| rs31618578 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80599161 | CTTTTTTCTCCATGA[A/G]GAAGAGAAGAACTCT | 17444 |
| rs31618579 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Grap2 | Mm_Celera | 15:80599394 | GCTATTCATAAACAA[C/T]GTGGTGGTTCGTAAA | 17444 |
| rs31618581 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80599470 | TGATGTTTAACCTGA[A/G]CCAGACCTTTAACAG | 17444 |
| rs31618583 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Grap2 | Mm_Celera | 15:80599488 | AGACCTTTAACAGAA[A/G]CGCAGAGTGAGACAA | 17444 |
| rs31618654 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Grap2 | Mm_Celera | 15:80580600 | GGAGTTAACACTACA[C/T]CCTACACTGAGTGTG | 17444 |
| rs31618656 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Grap2 | Mm_Celera | 15:80580699 | GAAGTTAACACTACA[C/T]CCTACACTGAGTGTG | 17444 |
| rs31618658 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Grap2 | Mm_Celera | 15:80580766 | GAGATAACACTACAC[C/T]TTACACTGAGAGTGA | 17444 |
| rs31618660 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Grap2 | Mm_Celera | 15:80580863 | TGGAGATAAGACTAC[A/T]CCCTACACTAAGTGT | 17444 |
| rs31618662 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80581054 | TTGCATATCTTAAAA[A/C]ATGCAGCATCTCATT | 17444 |
| rs31619492 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Grap2 | Mm_Celera | 15:80570614 | TTAAAGTGCTCTGTA[A/G]TGTGAAAACAGTGGC | 17444 |
| rs31619494 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80581090 | AATACCTCCCATGGT[C/T]CTTTCTTCTTTAACC | 17444 |
| rs31619496 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80581130 | CTGTGGCATTCTGGT[A/T]TCTTATAAATAGACC | 17444 |
| rs31619498 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80581191 | CAGCATTGTAAAACA[C/T]GTGGTACCCCACAAA | 17444 |
| rs31619500 | snp | A/T | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80581500 | AGAGATTACCTGTCC[A/T]GATTCTTTAACTCAT | 17444 |
| rs31619502 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80581575 | GAGGACCCGGATGAA[C/T]TGAGAACATTTAGGA | 17444 |
| rs31619565 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80599657 | TGTAAGCTGAGCAAC[A/G]CAATGCTTTAGAGCA | 17444 |
| rs31619567 | snp | A/G | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80599838 | GGAACCACTGTGTTT[A/G]AGAACCACGGCTTTA | 17444 |
| rs31619569 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80600001 | TTGTGCTTTGAGGTA[C/T]CTATCTGACAGCTCA | 17444 |
| rs31619571 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80600547 | CTTGAACCTCTACCT[A/G]CATTGTGGCAGCTTC | 17444 |
| rs31619573 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80600585 | TCTGTCCAAATCCTC[C/T]TTTGAGGCACAGGCA | 17444 |
| rs31620385 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Grap2 | Mm_Celera | 15:80600682 | TCTTTATCTCACTCT[A/G]GACGCCCCTAGTGAT | 17444 |
| rs31620387 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80600719 | GCCAGAGTCTCCCAA[C/T]TCTTTGTAGCAATTC | 17444 |
| rs31620389 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80600952 | TTGTCCTCTCAGGAA[A/G]TCTTCATGACCCTAG | 17444 |
| rs31620391 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80601826 | GGGTTTGTTTGTTTC[A/G]TCCTAAGTGCAACTG | 17444 |
| rs31620393 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Grap2 | Mm_Celera | 15:80602024 | CTGGTGGGAAAATGC[A/G]TCTCCATTTGTGAGC | 17444 |
| rs31620394 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Grap2 | Mm_Celera | 15:80581644 | GGAACGCACAATCTC[A/G]GGGAAAAGTAGGAGA | 17444 |
| rs31620396 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80582464 | ATTGGGTATCCAGAA[A/G]TTAAGTTTCTGTGAC | 17444 |
| rs31620398 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80582494 | CCGGAGCTCTTTTTG[A/T]AGAGGAACCTCTCTT | 17444 |
| rs31620400 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80583010 | TATTACATCTGACTA[G/T]AGTGATAGCAATGTG | 17444 |
| rs31620402 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80583022 | CTATAGTGATAGCAA[C/T]GTGTCAGAATATTCC | 17444 |
| rs31620454 | snp | A/G | 0.124444 | 0.216185 | upstream-variant-2KB | Grap2 | Mm_Celera | 15:80571524 | TGAGATACCGCCTCA[A/G]AAGTCAGGAATGAAG | 17444 |
| rs31620456 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Grap2 | Mm_Celera | 15:80571915 | TTGACCATAGCAAGC[C/T]TGGACTTAGAACCCC | 17444 |
| rs31620458 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Grap2 | Mm_Celera | 15:80572156 | ACTTTAACTTTTTCC[C/T]AGTGGCCTTTGCATT | 17444 |
| rs31620460 | snp | C/T | 0.124444 | 0.216185 | upstream-variant-2KB | Grap2 | Mm_Celera | 15:80572259 | AAACTCAGAAGTTTT[C/T]TTGTGTGAATGTGAG | 17444 |
| rs31620462 | snp | A/T | 0.408163 | 0.193609 | upstream-variant-2KB | Grap2 | Mm_Celera | 15:80572414 | TTCAACTCTAGCAGC[A/T]AGAAAACAAAACCAC | 17444 |
| rs31621144 | snp | A/C | 0.231111 | 0.249285 | utr-variant-5-prime | Grap2 | Mm_Celera | 15:80572700 | ATAACTCGTTGTCAA[A/C]GCCGAGATACACGCT | 17444 |
| rs31621146 | snp | G/T | 0.32 | 0.24 | utr-variant-5-prime | Grap2 | Mm_Celera | 15:80572733 | ACTCAACCTCTTCGC[G/T]TCCCAAAGGTAAGTC | 17444 |
| rs31621148 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80572859 | TCTGAACTTTGCTGG[C/T]AATACTTCAGCCATC | 17444 |
| rs31621150 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80572880 | TTCAGCCATCAGCCT[A/C]GGCTTCTTATCTAGT | 17444 |
| rs31621152 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80572903 | TATCTAGTTGGCTTA[C/T]GTTAGTAGGGATTGG | 17444 |
| rs31621164 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80583134 | GATAGCAGAGCAGCT[G/T]ATCTCACACTGCTCT | 17444 |
| rs31621166 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Grap2 | Mm_Celera | 15:80583149 | TATCTCACACTGCTC[C/T]CTGGCCTCAAAGGCT | 17444 |
| rs31621168 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80583198 | TCCTATCTGTGAGTG[C/T]CATCTGCAGCCCTGG | 17444 |
| rs31621170 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80583272 | ACAAGTGTGAGTGGC[C/T]GTTTCCTCTCCAAAC | 17444 |
| rs31621172 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80583287 | CGTTTCCTCTCCAAA[A/C]TTACACAAAGACTTA | 17444 |
| rs31621305 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80602078 | TGGAAATTGTTAATG[A/G]GGACTGTGTTATCGG | 17444 |
| rs31621307 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Grap2 | Mm_Celera | 15:80602106 | CGGCCCCCCTTAGTG[C/T]TCTGCCTGATAGAGA | 17444 |
| rs31621309 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80602145 | GTTCACCAGAGCAAT[C/T]CTGGAACCCTGATCA | 17444 |
| rs31621311 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Grap2 | Mm_Celera | 15:80602201 | GCTGACATAATCAAG[A/G]GAGTATAAATATATT | 17444 |
| rs31621313 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Grap2 | Mm_Celera | 15:80602245 | ATGGGGAAGGGAGAG[C/T]GCAGAAAGATTTGAG | 17444 |
| rs31621695 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80602318 | CCCAGTGTGTTGCCC[C/T]GTTGAGCAAAGGTGG | 17444 |
| rs31621697 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80602549 | CCGACTTGTTTAGCT[C/T]CTCTGCAGTTCAAAG | 17444 |
| rs31621699 | snp | C/T | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80602979 | GTCACTGCAGTGCAG[C/T]CGATCAAAGGCATGA | 17444 |
| rs31621701 | snp | C/T | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80603047 | TCTACCCTGGTCACA[C/T]GTTCATTGTTCTTTC | 17444 |
| rs31621703 | snp | A/G | 0.375 | 0.216506 | intron-variant | Grap2 | Mm_Celera | 15:80603096 | CGTCTCTCTACAGTG[A/G]TACCACCCGAGTAAG | 17444 |
| rs31621734 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80572936 | TCAACTTCTGTCAAA[C/T]GAACTAGAGAAAACT | 17444 |
| rs31621736 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Grap2 | Mm_Celera | 15:80573141 | TTGCTCAATTTTTTC[A/G]CCAACTCCAAACTGC | 17444 |
| rs31621738 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80573408 | CCACTTAACCTCAAG[C/T]GCAGCCTTGTTAATA | 17444 |
| rs31621740 | snp | C/T | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80573566 | ACTTCAGTGGAAGAG[C/T]CTTGCATATGGGTCC | 17444 |
| rs31621742 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Grap2 | Mm_Celera | 15:80574286 | AAAACGCATGATGGG[A/T]CCATTATTATTTCTC | 17444 |
| rs31621864 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80583362 | TATGAGAGGAGGAAA[C/T]GCTTTGTGCCAGGCT | 17444 |
| rs31621866 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Grap2 | Mm_Celera | 15:80583620 | GGTATAAAGAGCATG[C/T]GAATTAGGAATGGCT | 17444 |
| rs31621868 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Grap2 | Mm_Celera | 15:80584796 | TTTTAGGCTGAAACA[A/G]AGAGCTAGTGGGTGA | 17444 |
| rs31621870 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Grap2 | Mm_Celera | 15:80584812 | AGAGCTAGTGGGTGA[C/T]TTAGACAATTATATA | 17444 |
| rs31621872 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80585018 | GAGCATCTGGGACCT[A/G]GAGCTTCTGCGCTTG | 17444 |
| rs31622184 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80609025 | AGCCGAGGCTTAGTG[C/T]GCTTGGATAACTTTC | 17444 |
| rs31622186 | snp | C/T | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80609149 | GAGAGAGTGAGGTTA[C/T]TCAGCGTGACAGAGC | 17444 |
| rs31622188 | snp | A/T | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80609965 | GCTGAAGGCCTGACA[A/T]GATGATGAGAGAGGC | 17444 |
| rs31622190 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80610064 | GAAAGCACGCATCAG[A/G]AAGTGTCAGCCCACA | 17444 |
| rs31622192 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80610124 | TGAGATGTGGGAAGA[C/T]GGAAGGCCACAGCAG | 17444 |
| rs31622244 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80587929 | TGGCTTCAGCTGGCC[C/T]GTGCTACCAGAGCAA | 17444 |
| rs31622246 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80588003 | TCACTAACCAGCAGT[C/T]GCTGTCAAAAGGAAG | 17444 |
| rs31622248 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Grap2 | Mm_Celera | 15:80588509 | CAGCCTTATGCTACA[A/G]TTGTACAGCTTTGGA | 17444 |
| rs31622250 | snp | A/G | 0.375 | 0.216506 | intron-variant | Grap2 | Mm_Celera | 15:80588547 | GTGAACAGCTGATGT[A/G]CAGAGAGGCCTAGAC | 17444 |
| rs31622252 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Grap2 | Mm_Celera | 15:80588607 | GCTGTACCACCCTGT[G/T]AGGCAAACAGAGACA | 17444 |
| rs31622274 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80574812 | AGCATACGACGCACA[C/T]GTAAATAATAAATAA | 17444 |
| rs31622276 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Grap2 | Mm_Celera | 15:80574953 | GCGCCGCGCATCTCC[C/T]TATACAAAGGGGCGC | 17444 |
| rs31622278 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80574966 | CCCTATACAAAGGGG[C/T]GCCTCCATTTCGTGT | 17444 |
| rs31622280 | snp | C/T | 0.32 | 0.24 | intron-variant | Grap2 | Mm_Celera | 15:80575058 | CACAGCTTCATTCAA[C/T]GAACACGTCACTCAC | 17444 |
| rs31622282 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Grap2 | Mm_Celera | 15:80575142 | AACAACGTTCACAGT[A/G]GGTTTCAGTAGACTT | 17444 |
| rs31622355 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Grap2 | Mm_Celera | 15:80603249 | AGGCCCACCAAATAA[A/G]TCATCCAGGTGGCAG | 17444 |