Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs1222213359 | 0.574 | 0.720 | 6 | 43770966 | missense variant | G/A | snv | 62 | |||
rs267602852 | 0.827 | 0.160 | 11 | 32417631 | missense variant | G/A | snv | 7 | |||
rs2239785 | 0.827 | 0.240 | 22 | 36265284 | missense variant | G/A | snv | 0.79 | 0.68 | 5 | |
rs35366573 | 0.882 | 0.120 | 1 | 207785101 | missense variant | C/T | snv | 1.5E-02 | 1.5E-02 | 3 | |
rs1047763 | 0.925 | 0.120 | 7 | 7243938 | 3 prime UTR variant | G/A | snv | 0.22 | 2 | ||
rs373544789 | 0.925 | 0.120 | 19 | 54889688 | missense variant | G/A;T | snv | 8.8E-05; 3.2E-05 | 2 |