| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs193334346 | snp | A/C | 0.498698 | 0.025477 | intron-variant | helicase | WS195 | III:10431850 | AAATAAAATAGAAAA[A/C]AACTAGTTTTCAATT | 176462 |
| rs193334347 | snp | G/T | 0.01005 | 0.0701712 | intron-variant | helicase | WS195 | III:10433690 | TCCTCTATCTGGAAA[G/T]ATTCGAAAAATTGAT | 176462 |
| rs193334348 | snp | A/G | 0.0198 | 0.0975088 | missense | helicase | WS195 | III:10435577 | CCTTCTGCTTTTTTG[A/G]TTTTTTCTCTGAAAA | 176462 |
| rs193334349 | snp | C/T | 0.0198 | 0.0975088 | intron-variant | helicase | WS195 | III:10435594 | TTTTTCTCTGAAAAA[C/T]AGGAAAATAACAATG | 176462 |
| rs193600326 | snp | C/T | | | intron-variant | helicase | WS195 | III:10429594 | AATTTTCACTGAAAG[C/T]TTATAATAGTTTCGT | 176462 |
| rs193600327 | snp | A/T | | | intron-variant | helicase | WS195 | III:10431799 | GTCGATCTGAAAATT[A/T]AAAAAAAATTAAATT | 176462 |
| rs193600328 | snp | A/G | | | intron-variant | helicase | WS195 | III:10431806 | TGAAAATTAAAAAAA[A/G]ATTAAATTTTTTATT | 176462 |
| rs193600329 | snp | C/T | | | intron-variant | helicase | WS195 | III:10432001 | TTTATAATTTAAATA[C/T]ATTCTGTCGTGTCGA | 176462 |
| rs193600330 | snp | C/T | | | intron-variant | helicase | WS195 | III:10432136 | AATGCGGCGCATTTA[C/T]GTGCAATCAGGTGGC | 176462 |
| rs193600331 | snp | A/G | | | intron-variant | helicase | WS195 | III:10432998 | TCCCATTTTTTCTGG[A/G]AAAAAAAGCTCAGAT | 176462 |
| rs193600332 | snp | A/G | | | intron-variant | helicase | WS195 | III:10434394 | TTTTGCGTTTTTTCA[A/G]TAAAAAACGAAAAAA | 176462 |
| rs193600333 | snp | C/T | | | missense | helicase | WS195 | III:10435526 | CTTCACTAGGCATCG[C/T]CTCATCCACGTAATC | 176462 |
| rs353096189 | in-del | -/T | | | intron-variant | helicase | WS195 | III:10430963 | TAACAGAAATAAATA[-/T]TTTTTATTAGAGAAA | 176462 |
| rs353098372 | in-del | -/T | | | utr-variant-3-prime | helicase | WS195 | III:10428398 | ATAAAAATGATGAGA[-/T]TTTTTTTTGAAATGT | 176462 |
| rs353106718 | snp | G/T | | | intron-variant | helicase | WS195 | III:10434188 | AAAAATGGAATTTCC[G/T]CTGATTTTTATGATT | 176462 |
| rs353110526 | snp | G/T | | | missense | helicase | WS195 | III:10428753 | CTTCCTCTTTTTGCT[G/T]CTCTTTTTCGACAGG | 176462 |
| rs353117799 | snp | A/G | | | intron-variant | helicase | WS195 | III:10432098 | TCAACTCTGAGAGAG[A/G]GCAGCTGTCAAGTAA | 176462 |
| rs353134014 | in-del | -/A | | | intron-variant | helicase | WS195 | III:10430557 | AGAACCGAAAAACCG[-/A]AAAAAAAAATTGTAT | 176462 |
| rs353146941 | snp | A/T | | | intron-variant | helicase | WS195 | III:10429103 | TTAGTTTCAATAATT[A/T]AAAAAAAAAACGTAA | 176462 |
| rs353151295 | snp | G/T | | | missense | helicase | WS195 | III:10433103 | AATACGTGAGCAATT[G/T]GATACTCGGACACCA | 176462 |
| rs353154237 | snp | G/T | | | intron-variant | helicase | WS195 | III:10430771 | AATTTGTATAGTAAT[G/T]TTTTTCTGTAACTTT | 176462 |
| rs353165004 | in-del | -/T | | | intron-variant | helicase | WS195 | III:10435225 | AAATGTAAAAACCAG[-/T]TTTTTCCAAATTTTC | 176462 |
| rs353174188 | in-del | -/T | | | intron-variant | helicase | WS195 | III:10435063 | GAAATAATTTTTGCA[-/T]TTTTTTTTCATTTTC | 176462 |