Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 7 | |||
rs10830963 | 0.776 | 0.400 | 11 | 92975544 | intron variant | C/G | snv | 0.22 | 6 | ||
rs2943641 | 0.763 | 0.160 | 2 | 226229029 | intergenic variant | T/C | snv | 0.67 | 3 | ||
rs853789 | 2 | 168944978 | intron variant | A/G;T | snv | 0.75 | 3 | ||||
rs2877716 | 3 | 123375604 | intron variant | T/C | snv | 0.76 | 3 | ||||
rs5015480 | 0.851 | 0.120 | 10 | 92705802 | downstream gene variant | C/T | snv | 0.42 | 2 | ||
rs10423928 | 0.807 | 0.200 | 19 | 45679046 | intron variant | T/A | snv | 0.19 | 2 | ||
rs927332 | 6 | 6331640 | intergenic variant | T/C | snv | 0.48 | 1 | ||||
rs1800437 | 0.827 | 0.160 | 19 | 45678134 | missense variant | G/C | snv | 0.18 | 0.17 | 1 | |
rs12243326 | 0.925 | 0.160 | 10 | 113029056 | intron variant | T/C | snv | 0.27 | 1 | ||
rs17271305 | 15 | 62040781 | intron variant | A/G;T | snv | 1 |