| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193343486 | snp | A/C | 0.207153 | 0.246301 | missense | ? | WS195 | V:941001 | TGGAAATTTCTAGAT[A/C]CTTCTCTAGGCTGCT | 178599 |
| rs193343487 | snp | A/G | 0.019998 | 0.0979748 | intron-variant | ? | WS195 | V:943080 | CGCCCCCGCCTGCCT[A/G]CCTACCTGCCTCAAA | 178599 |
| rs193343488 | snp | G/T | 0.00999975 | 0.0699991 | intron-variant | ? | WS195 | V:943087 | GCCTGCCTGCCTACC[G/T]GCCTCAAATTTGTTA | 178599 |
| rs193343489 | snp | A/T | 0.00999975 | 0.0699991 | intron-variant | ? | WS195 | V:943143 | GCAAGTTTTCAAAAG[A/T]CTTTTTGAATTCCTA | 178599 |
| rs193343490 | snp | C/T | 0.00999975 | 0.0699991 | intron-variant | ? | WS195 | V:943144 | CAAGTTTTCAAAAGT[C/T]TTTTTGAATTCCTAC | 178599 |
| rs193343491 | snp | G/T | 0.0104709 | 0.0715948 | intron-variant | ? | WS195 | V:944497 | AATGAAACAATTATT[G/T]TTAAAAAAATTATTG | 178599 |
| rs193615026 | snp | A/G | | | missense | ? | WS195 | V:939838 | TGGTGGGATTGTTGA[A/G]CTGAAATTGAATGAA | 178599 |
| rs193615027 | snp | A/G | | | missense | ? | WS195 | V:940747 | GTTGGAAGCCACGTG[A/G]ATGATGCTGTGATGG | 178599 |
| rs193615028 | snp | A/T | | | intron-variant | ? | WS195 | V:941162 | AAATTTTAATTTTTT[A/T]AAAAATTCTTTATTA | 178599 |
| rs193615029 | snp | C/T | | | intron-variant | ? | WS195 | V:941719 | TTTTAAAAATTTCTT[C/T]AAAAAAGTAATTATT | 178599 |
| rs193615030 | snp | G/T | | | intron-variant | ? | WS195 | V:941746 | TATTTCTGAGAATTT[G/T]CGTTCCAAAATCCGG | 178599 |
| rs193615031 | snp | A/G | | | intron-variant | ? | WS195 | V:942473 | TCTGAAAATTTTCCG[A/G]ATTATTTTCTCCAAA | 178599 |
| rs193615032 | snp | A/C | | | intron-variant | ? | WS195 | V:943544 | TCCAAAATTAAAAAA[A/C]AAATTTTTTAGGGCG | 178599 |
| rs353123146 | in-del | -/T | | | intron-variant | ? | WS195 | V:941771 | ATCCGGAAAATCGAA[-/T]TTTTTTTCCCCGATT | 178599 |