| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193327461 | snp | A/C | 0.0771698 | 0.180637 | intron-variant | ? | WS195 | II:10237187 | AAAAACCGAAAAATA[A/C]AAATAAAAATTGAAG | 174587 |
| rs193327462 | snp | C/T | 0.0101008 | 0.0703445 | intron-variant | ? | WS195 | II:10237702 | TTTTTTCTTCCGAGT[C/T]CAAGAATGTGCTAAA | 174587 |
| rs193327463 | snp | C/T | 0.206241 | 0.24614 | intron-variant | ? | WS195 | II:10237786 | TACATCCATCTTTGC[C/T]TTTTTTTTCATTTTT | 174587 |
| rs193588464 | snp | A/G | | | intron-variant | ? | WS195 | II:10238304 | AAAAATACGGTAACC[A/G]GTCTCGGCACATAAT | 174587 |
| rs193588465 | snp | A/G | | | missense | ? | WS195 | II:10239153 | TCTTCACCATTTCGA[A/G]CGTTTTCAATGCTCC | 174587 |
| rs353115742 | snp | C/T | | | missense | ? | WS195 | II:10238171 | GACATGATTTATATG[C/T]TGTTGGAGAATATTC | 174587 |
| rs353117930 | snp | A/T | | | intron-variant | ? | WS195 | II:10238709 | TGCTGAATCTCAATT[A/T]AAAAAAAACTCACAA | 174587 |
| rs353125851 | snp | A/T | | | intron-variant | ? | WS195 | II:10237482 | TTTAGAAGTTTTTTT[A/T]AAATTTTTTCAATTA | 174587 |
| rs353142043 | snp | C/T | | | synonymous-codon | ? | WS195 | II:10237593 | CTGACTACGTGTTCC[C/T]GGGCTGTAGATCTGG | 174587 |
| rs353145637 | snp | A/T | | | intron-variant | ? | WS195 | II:10238216 | CATATTATTTTTTTT[A/T]AAATTTGATTCAAAA | 174587 |
| rs353156180 | snp | A/T | | | intron-variant | ? | WS195 | II:10238215 | TCATATTATTTTTTT[A/T]AAAATTTGATTCAAA | 174587 |
| rs353161298 | in-del | -/T | | | intron-variant | ? | WS195 | II:10237785 | TACATCCATCTTTGC[-/T]TTTTTTTTTCATTTT | 174587 |
| rs353175685 | snp | A/T | | | intron-variant | ? | WS195 | II:10238217 | ATATTATTTTTTTTA[A/T]AATTTGATTCAAAAA | 174587 |
| rs353180857 | in-del | -/T | | | intron-variant | ? | WS195 | II:10237786 | TACATCCATCTTTGC[-/T]TTTTTTTTCATTTTT | 174587 |