| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193348334 | snp | A/G | 0.01005 | 0.0701712 | intron-variant | sel-10 | WS195 | V:13818714 | TTGTGGTTGTAAATT[A/G]AATCACTTGTTTTAA | 179878 |
| rs193348335 | snp | A/T | 0.019998 | 0.0979748 | intron-variant | sel-10 | WS195 | V:13819875 | CCAAACCTTGAAGAG[A/T]GCACCTCAGCCAGGC | 179878 |
| rs193348336 | snp | C/T | 0.019998 | 0.0979748 | intron-variant | sel-10 | WS195 | V:13819880 | CCTTGAAGAGAGCAC[C/T]TCAGCCAGGCATATT | 179878 |
| rs193348337 | snp | A/G | 0.00999975 | 0.0699991 | missense, nc-transcript-variant | sel-10 | WS195 | V:13819995 | CTGCTTCAGGAATCC[A/G]ACATGACAAATATTC | 179878 |
| rs193348338 | snp | C/T | 0.0497189 | 0.149624 | intron-variant | sel-10 | WS195 | V:13821008 | CTTGATGGAAAGTTT[C/T]TGATTTGTAGATCAT | 179878 |
| rs193624567 | snp | A/G | | | intron-variant | sel-10 | WS195 | V:13819492 | CTAATTGAAATGTTT[A/G]TCTTCAGGACAATGG | 179878 |
| rs193624568 | snp | A/G | | | intron-variant | sel-10 | WS195 | V:13821216 | ACTTTCAACCCATAC[A/G]TTTTAATTTTAATAC | 179878 |