| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193325532 | snp | G/T | 0.019998 | 0.0979748 | missense | ? | WS195 | II:4423207 | ACGGAGAGGACTGAG[G/T]CCATTCGTTTTGTGT | 173778 |
| rs193586294 | snp | A/G | | | intron-variant | ? | WS195 | II:4422938 | ACTATTTTTCAGTGT[A/G]ATTGGCCAAAAATTC | 173778 |
| rs193586295 | snp | A/G | | | intron-variant | ? | WS195 | II:4423737 | GAATATTTCCGGCAA[A/G]TCGGCAATTTGCCGA | 173778 |
| rs193586296 | snp | C/T | | | synonymous-codon | ? | WS195 | II:4424091 | TTTCATCGTCACCTT[C/T]TTCAGTGGAACGTCT | 173778 |
| rs193586297 | snp | A/T | | | missense | ? | WS195 | II:4424125 | CGCGTGTCGAGCACG[A/T]AAATCGAACGATCTG | 173778 |
| rs193586298 | snp | A/T | | | intron-variant | ? | WS195 | II:4424571 | AAAATTGAAAAATAT[A/T]TTTTTCTAGAGATTT | 173778 |
| rs353126137 | in-del | -/GATTGTGGAGCT | | | cds-indel | ? | WS195 | II:4424363 | TTTCTGTTGTCCTTC[-/GATTGTGGAGCT]GATCTTCCAATATTT | 173778 |
| rs353131185 | snp | A/G | | | intron-variant | ? | WS195 | II:4423329 | GCAAACGATTTTTCC[A/G]GCAAATCACCAAATT | 173778 |
| rs353166905 | snp | A/G | | | intron-variant | ? | WS195 | II:4423552 | AATCAGAAATCCGAC[A/G]AATTTCCGAAATTGA | 173778 |