| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193320777 | snp | G/T | 0.00995 | 0.0698283 | missense | ? | WS195 | I:10259242 | GAAAGAATATGGTAT[G/T]TTGCTTGGCCCTAAA | 172894 |
| rs193320778 | snp | A/G | 0.00995 | 0.0698283 | intron-variant | ? | WS195 | I:10259289 | AAATAATTGTCAATA[A/G]AACAAATGCTTATCA | 172894 |
| rs193320779 | snp | A/T | 0.0198985 | 0.097741 | intron-variant | ? | WS195 | I:10261699 | GAAGATGAATGTAAA[A/T]TGAAAATATGACAAA | 172894 |
| rs193575607 | snp | C/T | | | utr-variant-3-prime | ? | WS195 | I:10255771 | AGCGAGCATTCATTG[C/T]TTTTCAGCTGAGCAG | 172894 |
| rs193575608 | snp | C/G | | | intron-variant | ? | WS195 | I:10261863 | GATTTGAATTTGATT[C/G]AAGCAATTGTGGATA | 172894 |
| rs353101527 | in-del | -/T | | | intron-variant | ? | WS195 | I:10259711 | TTAAATAAATTCTTG[-/T]TTTTTTTCGAGCAAG | 172894 |
| rs353143714 | snp | C/T | | | intron-variant | ? | WS195 | I:10256222 | TTATATATTTCTTTC[C/T]TTTTCTTTTTTCGAA | 172894 |