Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs25487 | 0.441 | 0.800 | 19 | 43551574 | missense variant | T/C | snv | 0.68 | 0.71 | 205 | |
rs759412116 | 0.581 | 0.640 | 19 | 45352210 | missense variant | C/G;T | snv | 4.0E-06; 6.0E-05 | 55 | ||
rs12190287 | 0.708 | 0.280 | 6 | 133893387 | 3 prime UTR variant | C/G;T | snv | 19 | |||
rs11553473 | 0.882 | 0.080 | 16 | 1314299 | missense variant | G/A | snv | 3 | |||
rs7187167 | 1.000 | 0.040 | 16 | 1299208 | upstream gene variant | T/C | snv | 0.69 | 2 | ||
rs121908690 | 0.925 | 0.080 | 1 | 46267540 | missense variant | G/A | snv | 1.4E-05 | 2 | ||
rs371228501 | 1.000 | 0.040 | 7 | 55191740 | missense variant | C/T | snv | 6.8E-05 | 1.2E-04 | 1 |