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 | |||
rs10719 | 0.677 | 0.680 | 5 | 31401340 | 3 prime UTR variant | A/G;T | snv | 0.69 | 24 | ||
rs7813 | 0.689 | 0.360 | 17 | 744946 | missense variant | G/A;C | snv | 0.63 | 22 | ||
rs868408509 | 0.827 | 0.160 | 6 | 128883315 | missense variant | C/G;T | snv | 4.6E-06 | 6 | ||
rs1991401 | 0.882 | 0.120 | 17 | 64506317 | 5 prime UTR variant | A/G | snv | 0.25 | 4 | ||
rs149146781 | 0.925 | 0.080 | 12 | 53314757 | missense variant | G/A;T | snv | 4.0E-06 | 2 | ||
rs768784941 | 0.925 | 0.080 | 12 | 53314352 | missense variant | G/A;C | snv | 4.0E-06 | 2 | ||
rs139819006 | 0.925 | 0.080 | 21 | 26022001 | missense variant | G/A | snv | 1.4E-04 | 6.3E-05 | 2 | |
rs771317418 | 0.925 | 0.080 | 21 | 26051117 | missense variant | A/G | snv | 2.0E-05 | 2.1E-05 | 2 | |
rs1297630698 | 0.925 | 0.080 | 2 | 162359540 | frameshift variant | C/- | del | 2 | |||
rs755258895 | 0.925 | 0.080 | 2 | 162347711 | missense variant | T/C | snv | 8.1E-06 | 2 | ||
rs1406402854 | 0.925 | 0.080 | 22 | 24614850 | missense variant | C/T | snv | 2 | |||
rs766007044 | 0.925 | 0.080 | 17 | 44385562 | missense variant | T/C | snv | 4.9E-06 | 2.1E-05 | 2 | |
rs137852604 | 0.925 | 0.080 | 10 | 110228276 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs759049323 | 0.925 | 0.080 | 10 | 110284872 | missense variant | T/C;G | snv | 4.0E-06; 4.0E-06 | 2 | ||
rs1224520731 | 0.925 | 0.080 | 2 | 37359620 | missense variant | T/C | snv | 4.0E-06 | 7.0E-06 | 2 | |
rs769267394 | 0.925 | 0.080 | 21 | 37153248 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs7005286 | 1.000 | 0.080 | 8 | 140584361 | intron variant | T/C | snv | 0.86 | 1 |