| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193359606 | snp | C/G | | | missense | ? | WS195 | III:8693608 | GGAAGCCTAATATAT[C/G]TGGGACATCTGGAAA | 176220 |
| rs193359607 | snp | A/G | | | synonymous-codon | ? | WS195 | III:8693612 | GCCTAATATATGTGG[A/G]ACATCTGGAAATTCA | 176220 |
| rs193359610 | snp | A/T | | | intron-variant | ? | WS195 | III:8693774 | ACCACTTTTCGAAAT[A/T]ATAATTTTGAGATAA | 176220 |
| rs353118460 | snp | C/T | | | missense | ? | WS195 | III:8698772 | GTGACGTCATCACAG[C/T]CCTGGAAGACATTGA | 176220 |
| rs353136001 | in-del | -/A | | | intron-variant | ? | WS195 | III:8693750 | TGTATTTTTGAAATG[-/A]AAAAAAAAACCACTT | 176220 |
| rs353148577 | snp | A/T | | | synonymous-codon | ? | WS195 | III:8698818 | CGCAGAATGTCGTGG[A/T]CAACAGGGAATGGTT | 176220 |
| rs353153890 | snp | G/T | | | utr-variant-3-prime | ? | WS195 | III:8699223 | CGATGCGTGTTTTGT[G/T]CCGATTGTCAAATTT | 176220 |
| rs353157165 | snp | A/G | | | intron-variant | ? | WS195 | III:8693921 | GGCAGCTTTATCGGA[A/G]AAGTTGAGACGACTA | 176220 |
| rs353165430 | snp | A/T | | | intron-variant | ? | WS195 | III:8697650 | AAAGATTAAAAAAAA[A/T]CAGATCAAACAAAAG | 176220 |
| rs353173187 | snp | A/G | | | synonymous-codon | ? | WS195 | III:8698923 | TGCATTCTCTCCGAA[A/G]AAGGCAGTTGCCACT | 176220 |
| rs353173886 | snp | A/T | | | intron-variant | ? | WS195 | III:8693663 | TGGTAAGTTTTTTTT[A/T]AAACTTTATGCTGAT | 176220 |
| rs353181599 | snp | A/T | | | intron-variant | ? | WS195 | III:8694134 | TATTGAAATTTTTTT[A/T]AAATTTCATTAAAAA | 176220 |