Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1016604233 | 1.000 | 0.080 | 7 | 139911241 | missense variant | C/T | snv | 8.0E-06 | 2.1E-05 | 1 | |
rs1033602309 | 1.000 | 0.080 | X | 9937279 | missense variant | G/C | snv | 1 | |||
rs1034429230 | 1.000 | 0.080 | 1 | 212365260 | missense variant | C/G | snv | 1.4E-05 | 1 | ||
rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
rs104894097 | 0.807 | 0.240 | 9 | 21974757 | missense variant | C/A;G;T | snv | 1.7E-05; 1.3E-05 | 1 | ||
rs1057519927 | 0.716 | 0.240 | 3 | 179218295 | missense variant | A/C;G;T | snv | 1 | |||
rs1057519981 | 0.689 | 0.440 | 17 | 7674251 | missense variant | A/C;G;T | snv | 1 | |||
rs1060502347 | 1.000 | 0.080 | 17 | 43091902 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs111265129 | 1.000 | 0.080 | 10 | 16851333 | missense variant | T/C | snv | 3.3E-03 | 1.3E-02 | 1 | |
rs111299050 | 1.000 | 0.080 | 11 | 31370815 | missense variant | A/G | snv | 4.3E-04 | 2.2E-03 | 1 | |
rs111367604 | 1.000 | 0.080 | 2 | 214728927 | missense variant | C/A;G;T | snv | 8.0E-06 | 1 | ||
rs112523432 | 1.000 | 0.080 | 1 | 214384776 | missense variant | T/C;G | snv | 4.0E-06; 5.9E-03 | 1 | ||
rs112973609 | 1.000 | 0.080 | 11 | 120118309 | missense variant | G/A | snv | 2.0E-05 | 1 | ||
rs113117391 | 1.000 | 0.080 | 8 | 52628128 | missense variant | G/A | snv | 2.2E-04 | 2.5E-04 | 1 | |
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
rs113776284 | 1.000 | 0.080 | 2 | 227893863 | missense variant | C/T | snv | 3.6E-05 | 3.5E-05 | 1 | |
rs11540652 | 0.592 | 0.640 | 17 | 7674220 | missense variant | C/A;G;T | snv | 1.2E-05 | 1 | ||
rs11571747 | 1.000 | 0.080 | 13 | 32371035 | missense variant | A/C | snv | 1.1E-03 | 1.5E-03 | 1 | |
rs11571769 | 1.000 | 0.080 | 13 | 32379413 | missense variant | G/A;T | snv | 9.5E-03 | 8.2E-03 | 1 | |
rs116076204 | 1.000 | 0.080 | 18 | 45870626 | missense variant | G/A;C | snv | 7.1E-04; 1.2E-05 | 1 | ||
rs11643870 | 1.000 | 0.080 | 16 | 84318346 | missense variant | G/A | snv | 8.8E-03 | 8.4E-03 | 1 | |
rs1165078436 | 1.000 | 0.080 | 1 | 31798459 | missense variant | G/A | snv | 4.0E-06 | 7.0E-06 | 1 | |
rs1165723137 | 1.000 | 0.080 | 19 | 47839489 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
rs1165948169 | 1.000 | 0.080 | 12 | 47798799 | missense variant | C/T | snv | 1 | |||
rs116967198 | 1.000 | 0.080 | 18 | 13681833 | missense variant | C/A;T | snv | 4.0E-06; 1.2E-05 | 1 |