Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121907896 | 0.851 | 0.200 | 11 | 64591825 | missense variant | G/A | snv | 1.8E-04 | 8.4E-05 | 5 | |
rs1451506414 | 0.882 | 0.200 | 11 | 64598561 | synonymous variant | G/A | snv | 4 | |||
rs753482595 | 0.925 | 0.200 | 4 | 9920389 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 3 | |
rs561633150 | 0.925 | 0.200 | 4 | 9980627 | missense variant | C/T | snv | 6.1E-04 | 9.1E-05 | 2 | |
rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 107 | ||
rs1800471 | 0.597 | 0.840 | 19 | 41352971 | missense variant | C/G;T | snv | 5.6E-02 | 48 | ||
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 |