Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs863223904 | 0.827 | 0.200 | X | 55014829 | missense variant | C/T | snv | 6.1E-06 | 5 | ||
rs80356713 | 0.925 | 0.120 | X | 75070499 | missense variant | C/A;G | snv | 3 | |||
rs201062903 | 0.882 | 0.120 | X | 55013527 | missense variant | G/A | snv | 1.3E-03 | 1.2E-03 | 3 | |
rs541845688 | 0.925 | 0.160 | 2 | 219210782 | missense variant | C/T | snv | 4.4E-05 | 7.0E-06 | 2 | |
rs797044558 | 0.925 | 0.160 | X | 75053585 | missense variant | C/T | snv | 2 | |||
rs1557248142 | 0.925 | 0.080 | X | 55021182 | missense variant | G/T | snv | 2 | |||
rs892041887 | 0.925 | 0.080 | X | 55009265 | missense variant | C/T | snv | 2 | |||
rs1460260991 | 1.000 | 0.040 | 3 | 52203996 | synonymous variant | A/G | snv | 4.1E-06 | 1 | ||
rs200361165 | 1.000 | 0.040 | 3 | 52212412 | missense variant | A/C;G | snv | 1.2E-05 | 1 |