| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs45828026 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650499 | CAACTCATGTAAGAA[A/C]AAAAGATGGATGTAA | 100042786 |
| rs47496654 | snp | A/T | | | intron-variant | Gm16381 | GRCm38.p3 | 12:87644762 | AAAGCACTCGAACAC[A/T]GAAAGATGAAGATGA | 100042786 |
| rs48179851 | snp | A/G | 0.497778 | 0.0332592 | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650732 | TCTGCCTGCCAAGAA[A/G]CATCCAACAACAACT | 100042786 |
| rs48963239 | snp | A/C/G/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650181 | TAATCCGAGGACTCT[A/C/G/T]AGTTCAATGTCAGCC | 100042786 |
| rs49127080 | snp | C/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650130 | GTCTATATATAGTGG[C/T]ACACACCTTTAATCT | 100042786 |
| rs49465730 | snp | A/G | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650230 | AGGTAATGGCCATGA[A/G]AAACTTAGGCCCAGG | 100042786 |
| rs49517315 | snp | G/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650617 | TGTGGCGTTTGTTGT[G/T]CTGGGTGCCCTCTGT | 100042786 |
| rs50123772 | snp | C/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650696 | CAGGCTTTACCTGCC[C/T]GTGGATCTTTGAGAG | 100042786 |
| rs50820055 | snp | A/G | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650112 | ACACCTTTAATCTAG[A/G]CCACACCTTCTGCTA | 100042786 |
| rs51330052 | snp | A/G | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650153 | GCCTGGGACAAAGCA[A/G]GTCCCAGGTCTATAT | 100042786 |
| rs51492811 | snp | A/C/G/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650393 | TCACTGCAACTTCCT[A/C/G/T]ACAACTTTGAGTTTC | 100042786 |
| rs51949822 | snp | G/T | | | intron-variant | Gm16381 | GRCm38.p3 | 12:87644761 | AAGCACTCGAACACT[G/T]AAAGATGAAGATGAA | 100042786 |
| rs107918007 | snp | C/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650892 | TTTTGGTTTTTTTTT[C/T]TTTCTTTCTTTCTTT | 100042786 |
| rs108073605 | snp | G/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650880 | TGGTTTTTGTTTTTT[G/T]GGTTTTTTTTTTTTT | 100042786 |
| rs108261610 | snp | C/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650964 | CTGTCCTGGAACTCA[C/T]TTTGTAGACCAGGCT | 100042786 |
| rs108390908 | snp | A/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650766 | AAGGTCTGAATATGG[A/T]TAGCCTAGGGAGTGG | 100042786 |
| rs108761184 | snp | A/G | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650742 | AAGAAGCATCCAACA[A/G]CAACTGTCAAGGTCT | 100042786 |
| rs108889507 | snp | G/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650707 | CCACAGGCAGGTAAA[G/T]CCTGAATTGTCTGCC | 100042786 |
| rs219568881 | snp | A/C | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650292 | CAATTTACAAAAAAA[A/C]CCAAAACCAAAAAAA | 100042786 |
| rs220422926 | snp | A/G | | | intron-variant | Gm16381 | GRCm38.p3 | 12:87645550 | TAGATAGGTAGATAG[A/G]TAGATAGATAGATAG | 100042786 |
| rs223944445 | snp | A/C | | | intron-variant | Gm16381 | GRCm38.p3 | 12:87645306 | TTAAAATACTCAAAC[A/C]AAAAAAAAAAAAAAG | 100042786 |
| rs242370284 | snp | C/T | | | intron-variant | Gm16381 | GRCm38.p3 | 12:87645417 | CCACAAGTAAAGGAA[C/T]CTAATTTCTTTCCTA | 100042786 |
| rs246051305 | snp | A/G | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650142 | TGTACCACTATATAT[A/G]GACCTGGGACCTGCT | 100042786 |
| rs250677119 | snp | C/T | | | intron-variant | Gm16381 | GRCm38.p3 | 12:87645439 | TCTTTCCTACTTGTC[C/T]ATCTTTAAAATAACA | 100042786 |
| rs387173856 | in-del | -/G | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650340 | CCTTAAAAAAAGCCA[-/G]AAGACCTAACTTCTC | 100042786 |
| rs579194454 | snp | A/C | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650273 | TGTCAGCCCTGGTCC[A/C]CAGCAATTTACAAAA | 100042786 |
| rs579647999 | snp | A/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650420 | GTGAGCTGACAGGGC[A/T]GAGGAGGAGGTTGCT | 100042786 |
| rs580172822 | snp | C/G | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650438 | GGAGGAGGTTGCTCA[C/G]TCAGTGCAGTACTCA | 100042786 |
| rs580868317 | snp | A/C/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650938 | GACAGGGTTTCCCTA[A/C/T]ATAGCCCTGGCTGTC | 100042786 |
| rs581481167 | snp | A/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650601 | CAAGCAAACTTGCCC[A/T]ACAGAGGGCACCCAG | 100042786 |
| rs582642694 | snp | C/T | | | intron-variant | Gm16381 | GRCm38.p3 | 12:87645280 | TTCTAGTTACACTTC[C/T]ATTGCTGCTGTTAAA | 100042786 |
| rs582650183 | snp | A/G | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650344 | TAAAAAAAGCCAAAG[A/G]CCTAACTTCTCTCTG | 100042786 |
| rs583417654 | snp | A/G | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650424 | GCTGACAGGGCTGAG[A/G]AGGAGGTTGCTCACT | 100042786 |
| rs583660639 | snp | C/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650487 | TTGAGTTCAATGCAA[C/T]TCATGTAAGAAAAAA | 100042786 |
| rs585896265 | snp | G/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650433 | GCTGAGGAGGAGGTT[G/T]CTCACTCAGTGCAGT | 100042786 |
| rs586631204 | snp | C/T | | | upstream-variant-2KB | Gm16381 | GRCm38.p3 | 12:87650636 | ACAAACGCCACATGC[C/T]CAGTGTGTCTGTGCT | 100042786 |