| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193322586 | snp | G/T | 0.239198 | 0.249766 | intron-variant | ? | WS195 | I:13590162 | CAGTTTTTGGTTGAG[G/T]CTGAAAAATTGTGTA | 190778 |
| rs193578781 | snp | A/C | | | intron-variant | ? | WS195 | I:13597581 | TGTAATCTCCCACAT[A/C]TTCATCTCCCTTTTC | 190778 |
| rs353100958 | snp | G/T | | | intron-variant | ? | WS195 | I:13594089 | CAACCAAATTCTAGT[G/T]TTTTTTTCTAAGTGT | 190778 |
| rs353105533 | in-del | -/T | | | intron-variant | ? | WS195 | I:13592363 | TAAAGAAAATTTTCG[-/T]TTTTTTTTTTTTTTG | 190778 |
| rs353131518 | snp | A/T | | | intron-variant | ? | WS195 | I:13594657 | AGTCAAAACTAGTTT[A/T]TTTCTGAATTTTTCA | 190778 |
| rs353132733 | snp | A/T | | | missense | ? | WS195 | I:13593573 | ACCATTTTCCATGTT[A/T]AAAAGTTGAATTTCC | 190778 |
| rs353150508 | snp | A/G | | | intron-variant, missense | ?, Y87G2A.12 | WS195 | I:13596579 | TGCAACCAATCGGAA[A/G]TGAGCAGTACAGAAA | 190778 |
| rs353157392 | in-del | -/A | | | intron-variant | ? | WS195 | I:13598287 | AACTTGTTAACCTGC[-/A]AAAAAAAAACATGTT | 190778 |