Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1801725 | 0.633 | 0.600 | 3 | 122284910 | missense variant | G/T | snv | 0.13 | 0.11 | 39 | |
rs2282679 | 0.645 | 0.480 | 4 | 71742666 | intron variant | T/G | snv | 0.21 | 38 | ||
rs137854539 | 0.716 | 0.520 | 20 | 58903703 | missense variant | C/T | snv | 28 | |||
rs75076352 | 0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 | 24 | ||
rs1042636 | 0.672 | 0.360 | 3 | 122284922 | missense variant | A/G | snv | 0.15 | 9.0E-02 | 23 | |
rs75996173 | 0.716 | 0.240 | 10 | 43114501 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 21 | ||
rs78014899 | 0.742 | 0.160 | 10 | 43118392 | missense variant | G/A;C;T | snv | 8.0E-06 | 12 | ||
rs377767404 | 0.742 | 0.160 | 10 | 43114488 | missense variant | T/C | snv | 11 | |||
rs104893689 | 0.790 | 0.200 | 3 | 122261589 | missense variant | G/A;C | snv | 10 | |||
rs193922442 | 0.827 | 0.120 | 3 | 122261589 | frameshift variant | G/- | del | 5 | |||
rs767363250 | 0.827 | 0.280 | 3 | 122283992 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 5 | |
rs61734277 | 0.882 | 0.080 | 6 | 10874672 | missense variant | A/C | snv | 9.1E-03 | 8.6E-03 | 5 | |
rs201858689 | 0.882 | 0.120 | 3 | 122284257 | missense variant | G/T | snv | 2.8E-05 | 3 | ||
rs6254 | 0.925 | 0.080 | 11 | 13492716 | intron variant | C/A;T | snv | 4.0E-06; 0.28 | 2 |