Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs2273535 | 0.645 | 0.360 | 20 | 56386485 | missense variant | A/C;T | snv | 0.28 | 37 | ||
rs121913227 | 0.653 | 0.320 | 7 | 140753336 | missense variant | AC/CT;TT | mnv | 31 | |||
rs1047972 | 0.716 | 0.240 | 20 | 56386407 | missense variant | T/C | snv | 0.85 | 0.84 | 19 | |
rs11249433 | 0.827 | 0.160 | 1 | 121538815 | intron variant | A/C;G | snv | 8 | |||
rs1043994 | 0.827 | 0.120 | 19 | 15192033 | synonymous variant | T/A;C | snv | 4.0E-06; 0.85 | 7 | ||
rs3124591 | 0.827 | 0.120 | 9 | 136495945 | 3 prime UTR variant | C/T | snv | 0.62 | 6 | ||
rs3815188 | 0.827 | 0.120 | 19 | 15192414 | synonymous variant | G/A;T | snv | 0.17 | 6 | ||
rs367398 | 0.827 | 0.160 | 6 | 32223953 | 5 prime UTR variant | G/A | snv | 0.34 | 0.40 | 5 | |
rs520692 | 0.882 | 0.120 | 6 | 32220863 | missense variant | T/C | snv | 0.31 | 0.29 | 3 | |
rs780881510 | 0.925 | 0.080 | 17 | 39715299 | missense variant | A/C | snv | 1.2E-05 | 2 | ||
rs145459032 | 1.000 | 0.080 | 7 | 106867607 | missense variant | A/C;G | snv | 2.0E-05 | 2.1E-05 | 1 |