Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 24 | ||
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 10 | |||
rs174548 | 0.851 | 0.160 | 11 | 61803876 | 5 prime UTR variant | C/G;T | snv | 9 | |||
rs174576 | 0.851 | 0.200 | 11 | 61836038 | intron variant | C/A;T | snv | 9 | |||
rs599839 | 0.724 | 0.360 | 1 | 109279544 | downstream gene variant | G/A;C | snv | 9 | |||
rs630014 | 9 | 133274306 | intron variant | G/A;C | snv | 9 | |||||
rs174601 | 0.925 | 0.080 | 11 | 61855668 | non coding transcript exon variant | C/A;T | snv | 8 | |||
rs11206510 | 0.763 | 0.240 | 1 | 55030366 | intergenic variant | T/A;C;G | snv | 7 | |||
rs445925 | 0.882 | 0.080 | 19 | 44912383 | non coding transcript exon variant | G/A;C | snv | 7 | |||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 7 | |||
rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 7 | |||
rs676210 | 0.925 | 0.120 | 2 | 21008652 | missense variant | G/A;T | snv | 0.29 | 7 | ||
rs11570255 | 1.000 | 20 | 59300861 | missense variant | G/A;T | snv | 3.3E-03; 2.9E-05 | 6 | |||
rs11571151 | 11 | 101127486 | missense variant | C/G;T | snv | 6 | |||||
rs1169288 | 0.776 | 0.160 | 12 | 120978847 | missense variant | A/C;T | snv | 0.35 | 6 | ||
rs17240378 | 16 | 67942790 | intron variant | G/C;T | snv | 4.0E-06 | 6 | ||||
rs2001945 | 8 | 125465736 | upstream gene variant | G/A;C;T | snv | 6 | |||||
rs2228671 | 0.790 | 0.160 | 19 | 11100236 | stop gained | C/A;G;T | snv | 1.6E-05; 8.9E-02 | 6 | ||
rs2980875 | 8 | 125469505 | intron variant | A/C;G;T | snv | 6 | |||||
rs3093267 | 13 | 113118661 | missense variant | G/A;T | snv | 8.0E-05 | 6 | ||||
rs33980385 | 19 | 40991388 | missense variant | A/G | snv | 6 | |||||
rs4299376 | 0.851 | 0.120 | 2 | 43845437 | intron variant | G/C;T | snv | 6 | |||
rs519113 | 1.000 | 0.080 | 19 | 44873027 | intron variant | C/G;T | snv | 6 | |||
rs9341023 | 6 | 152062578 | intron variant | C/T | snv | 6 | |||||
rs10789117 | 1 | 62606594 | intron variant | A/C;T | snv | 5 |