Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs1188383936 | 0.524 | 0.760 | 11 | 46725976 | missense variant | C/T | snv | 8.0E-06 | 102 | ||
rs899127658 | 0.547 | 0.720 | 11 | 46739084 | missense variant | G/A;C | snv | 82 | |||
rs751377893 | 0.574 | 0.680 | 1 | 169546513 | missense variant | T/C | snv | 4.0E-06 | 65 | ||
rs6025 | 0.637 | 0.560 | 1 | 169549811 | missense variant | C/T | snv | 1.8E-02 | 43 | ||
rs1799963 | 0.695 | 0.400 | 11 | 46739505 | 3 prime UTR variant | G/A | snv | 9.6E-03 | 25 | ||
rs552953108 | 0.724 | 0.200 | 11 | 46729529 | missense variant | G/A | snv | 1.6E-05 | 4.2E-05 | 16 | |
rs368927897 | 0.790 | 0.240 | 9 | 5072541 | missense variant | G/A;T | snv | 2.8E-05; 6.4E-05 | 9 | ||
rs387906674 | 0.925 | 0.040 | 3 | 93893025 | missense variant | G/A | snv | 2.0E-05 | 2 | ||
rs6123 | 0.925 | 0.080 | 3 | 93874275 | synonymous variant | T/C | snv | 0.43 | 0.34 | 2 | |
rs963668412 | 0.925 | 0.040 | 3 | 93927362 | missense variant | C/T | snv | 8.0E-06 | 1.4E-05 | 2 | |
rs1328295730 | 1.000 | 0.040 | 3 | 93906074 | missense variant | G/A | snv | 1 | |||
rs753950548 | 1.000 | 0.040 | 3 | 93910654 | missense variant | G/T | snv | 1.4E-05 | 1 | ||
rs1022228924 | 1.000 | 0.040 | 17 | 7630506 | missense variant | A/G | snv | 1 |