| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193325836 | snp | A/G | 0.0198985 | 0.097741 | intron-variant | ? | WS195 | II:5391587 | GCATCCAAAAAAATT[A/G]ATTGATTCATTGCCC | 173917 |
| rs193325837 | snp | G/T | 0.0198985 | 0.097741 | intron-variant | ? | WS195 | II:5391591 | CCAAAAAAATTAATT[G/T]ATTCATTGCCCGAGA | 173917 |
| rs193325838 | snp | A/G | 0.0198 | 0.0975088 | intron-variant | ? | WS195 | II:5392435 | TCGTTAGTATAACTT[A/G]AACCTACATGTTCCT | 173917 |
| rs193586739 | snp | A/T | | | intron-variant | ? | WS195 | II:5391763 | GTTTTTAAATCAACA[A/T]TTTTTTTTTGGTCCA | 173917 |
| rs193586740 | snp | A/G | | | intron-variant | ? | WS195 | II:5392949 | TAAAATTTGATCTAT[A/G]TACCATAACTCCAAT | 173917 |
| rs353096329 | in-del | -/T | | | intron-variant | ? | WS195 | II:5391708 | AGCCTCAAAACATTC[-/T]TTTTTTTTGTTTCCA | 173917 |
| rs353125641 | snp | A/G | | | missense | ? | WS195 | II:5392141 | TACATAGAATTGCAA[A/G]AACACTATCATCCAT | 173917 |
| rs353158532 | snp | A/T | | | intron-variant | ? | WS195 | II:5391221 | TTTATAAATTTTCTG[A/T]ATAGAATGAAAAGGC | 173917 |