Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 19 | ||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 17 | |||
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 17 | ||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs11556924 | 0.752 | 0.240 | 7 | 130023656 | missense variant | C/A;T | snv | 4.0E-06; 0.28 | 13 | ||
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
rs3840870 | 17 | 50184820 | 3 prime UTR variant | -/CTTG | delins | 13 | |||||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs198851 | 6 | 26104404 | downstream gene variant | T/A;C;G | snv | 11 | |||||
rs140522 | 0.851 | 0.160 | 22 | 50532837 | upstream gene variant | T/A;C | snv | 10 | |||
rs76428106 | 0.851 | 0.040 | 13 | 28029870 | intron variant | T/C;G | snv | 10 | |||
rs8176746 | 0.882 | 0.160 | 9 | 133255935 | missense variant | G/A;T | snv | 4.1E-06; 0.12 | 6 | ||
rs9349205 | 6 | 41957421 | intron variant | G/A;C | snv | 6 | |||||
rs445925 | 0.882 | 0.080 | 19 | 44912383 | non coding transcript exon variant | G/A;C | snv | 5 | |||
rs4672497 | 2 | 62296430 | TF binding site variant | C/G;T | snv | 5 | |||||
rs55709272 | 2 | 113109711 | intron variant | T/A;C | snv | 5 | |||||
rs66505542 | 11 | 116752498 | intron variant | AA/-;A;AAA | delins | 5 | |||||
rs755249 | 1 | 39529402 | 3 prime UTR variant | C/A;T | snv | 5 | |||||
rs77960347 | 18 | 49583585 | missense variant | A/C;G | snv | 4.0E-06; 8.7E-03 | 5 | ||||
rs9411378 | 9 | 133270015 | intron variant | A/C;T | snv | 5 | |||||
rs11021221 | 11 | 95575690 | intron variant | T/A;G | snv | 4 | |||||
rs11756659 | 6 | 25933704 | upstream gene variant | A/G;T | snv | 4 | |||||
rs12459419 | 0.925 | 0.120 | 19 | 51225221 | missense variant | C/G;T | snv | 0.31 | 4 | ||
rs144204502 | 17 | 78187152 | 5 prime UTR variant | C/G;T | snv | 1.2E-02 | 4 | ||||
rs1958078 | 14 | 69888141 | intron variant | A/C;G | snv | 4 |