Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1042522 | 0.426 | 0.800 | 17 | 7676154 | missense variant | G/C;T | snv | 0.67 | 242 | ||
rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
rs28934571 | 0.645 | 0.360 | 17 | 7674216 | missense variant | C/A;G | snv | 31 | |||
rs28934573 | 0.667 | 0.480 | 17 | 7674241 | missense variant | G/A;C;T | snv | 4.0E-06 | 28 | ||
rs121913400 | 0.683 | 0.360 | 3 | 41224610 | missense variant | C/A;G;T | snv | 26 | |||
rs121913409 | 0.708 | 0.400 | 3 | 41224646 | missense variant | C/A;G;T | snv | 21 | |||
rs121913412 | 0.724 | 0.280 | 3 | 41224633 | missense variant | A/C;G;T | snv | 19 | |||
rs28931588 | 0.701 | 0.200 | 3 | 41224606 | missense variant | G/A;C;T | snv | 17 | |||
rs28931589 | 0.695 | 0.240 | 3 | 41224613 | missense variant | G/A;C;T | snv | 17 | |||
rs11655237 | 0.724 | 0.280 | 17 | 72404025 | non coding transcript exon variant | C/T | snv | 0.16 | 17 | ||
rs28933386 | 0.752 | 0.400 | 12 | 112477719 | missense variant | A/G | snv | 1.2E-05 | 7.0E-06 | 15 | |
rs137854573 | 0.807 | 0.120 | 5 | 112828889 | stop gained | C/T | snv | 10 | |||
rs762471803 | 0.925 | 0.040 | 11 | 102114201 | missense variant | T/G | snv | 6 | |||
rs137854574 | 0.925 | 0.120 | 5 | 112828919 | stop gained | C/T | snv | 4 | |||
rs768298443 | 1.000 | 0.040 | 10 | 112950932 | missense variant | C/A | snv | 4.1E-06 | 2 | ||
rs780571021 | 1.000 | 0.040 | 10 | 113146069 | missense variant | G/C;T | snv | 4.0E-06; 8.0E-06 | 2 | ||
rs781124288 | 1.000 | 0.040 | 4 | 168139494 | missense variant | A/G | snv | 4.0E-06 | 1 | ||
rs137854578 | 1.000 | 0.040 | 5 | 112839777 | missense variant | A/T | snv | 1 | |||
rs202128953 | 1.000 | 0.040 | 11 | 20364346 | stop gained | G/A;T | snv | 7.2E-05 | 1 | ||
rs763708092 | 1.000 | 0.040 | 1 | 204549443 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 1 | |
rs983496580 | 1.000 | 0.040 | 1 | 204526387 | missense variant | A/G | snv | 1 | |||
rs1389001294 | 1.000 | 0.040 | 3 | 50331640 | missense variant | C/T | snv | 1.4E-05 | 1 |