| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193319309 | snp | C/T | 0.0296962 | 0.118179 | utr-variant-3-prime | ? | WS195 | I:3920286 | TTTAAAGGGTTCACG[C/T]GTTTTTTAAACACTC | 171978 |
| rs193319310 | snp | A/T | 0.0296962 | 0.118179 | utr-variant-3-prime | ? | WS195 | I:3920308 | TAAACACTCATTGAA[A/T]TTATTTCTAAATAAA | 171978 |
| rs193319311 | snp | A/C | 0.0198985 | 0.097741 | utr-variant-3-prime | ? | WS195 | I:3920372 | CAAATTAAACTATTT[A/C]GAATTCACAAATAGT | 171978 |
| rs193319312 | snp | A/G | 0.020831 | 0.0999079 | intron-variant | ? | WS195 | I:3923424 | AAAAAAAAACCAAAG[A/G]CCATTTTCTGAGGAA | 171978 |
| rs193573326 | snp | C/T | | | utr-variant-3-prime | ? | WS195 | I:3920280 | TTCTTTTTTAAAGGG[C/T]TCACGCGTTTTTTAA | 171978 |
| rs353109846 | snp | C/T | | | intron-variant | ? | WS195 | I:3923866 | AGTCTCAAATTCCAA[C/T]TTTTTTCGTTTTTCA | 171978 |
| rs353113722 | in-del | -/A | | | intron-variant | ? | WS195 | I:3923793 | GCTCTAACAATGCTG[-/A]AAAAAAAATCGATTT | 171978 |
| rs353128105 | snp | C/T | | | missense | ? | WS195 | I:3923737 | GACACTCGGTACATT[C/T]CACAGCTTCCGGCTC | 171978 |
| rs353174823 | snp | A/G | | | intron-variant | ? | WS195 | I:3922253 | GGGTTGCAAAATTAC[A/G]CCCCGCCTTTCTTTC | 171978 |