| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193319956 | snp | A/T | 0.02955 | 0.117906 | intron-variant | ? | WS195 | I:6480597 | GTGACTTTGGAAAAA[A/T]GTTTTATAAATGTAA | 172355 |
| rs193319957 | snp | G/T | 0.0296962 | 0.118179 | intron-variant | ? | WS195 | I:6480598 | TGACTTTGGAAAAAT[G/T]TTTTATAAATGTAAT | 172355 |
| rs193319958 | snp | A/T | 0.10395 | 0.202902 | intron-variant | ?, sulp-1 | WS195 | I:6483095 | AATTAATATACAATC[A/T]AACATTTCAGTTGGT | 172355 |
| rs193574170 | snp | A/C | | | missense, intron-variant | ? | WS195 | I:6476112 | TGCAAATTCTGTGGA[A/C]TCAGATTTCGGAAAA | 172355 |
| rs193574171 | snp | C/T | | | utr-variant-3-prime, synonymous-codon | ? | WS195 | I:6477292 | TGATACTAATAATTT[C/T]CCATTTGGATCTACA | 172355 |
| rs193574172 | snp | G/T | | | intron-variant | ? | WS195 | I:6481442 | TTTTTCCATAAATTA[G/T]GTTTTAAATATTTGT | 172355 |
| rs193574173 | snp | C/T | | | intron-variant, missense | ?, sulp-1 | WS195 | I:6482627 | TATCAATCACCAAAT[C/T]CATGGACACAGATTC | 172355 |
| rs193574174 | snp | C/T | | | synonymous-codon, intron-variant | sulp-1, ? | WS195 | I:6483248 | TCTTCAATGCTTTTA[C/T]GCAGCTGTTCCATGT | 172355 |
| rs353100084 | snp | C/T | | | intron-variant | ? | WS195 | I:6480793 | TTCAAGAAATTTAAG[C/T]TCGTATTCTTTTTCC | 172355 |
| rs353112902 | in-del | -/T | | | intron-variant | ? | WS195 | I:6479879 | CATACTCATTTGCTC[-/T]TTTTTTTTTCATTTT | 172355 |
| rs353119479 | in-del | -/T | | | intron-variant | ? | WS195 | I:6480231 | CGTTTCCTCTCAAAC[-/T]TTTTTTTTTTTGACG | 172355 |
| rs353161150 | in-del | -/A | | | intron-variant | ? | WS195 | I:6481621 | ATTTTGAAAGGTTTC[-/A]AAAAAAAAAAACGGA | 172355 |