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 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs34637584 | 0.583 | 0.480 | 12 | 40340400 | missense variant | G/A | snv | 5.3E-04 | 3.6E-04 | 78 | |
rs972936 | 0.807 | 0.200 | 12 | 102431143 | intron variant | T/C | snv | 0.70 | 12 | ||
rs7136446 | 0.882 | 0.160 | 12 | 102444737 | intron variant | C/T | snv | 0.66 | 8 | ||
rs3743077 | 1.000 | 0.040 | 15 | 78602554 | intron variant | C/T | snv | 0.31 | 3 | ||
rs16979956 | X | 15525068 | intron variant | C/T | snv | 4.0E-04 | 2 | ||||
rs35697037 | X | 15523993 | intron variant | G/A | snv | 0.37 | 2 | ||||
rs2304297 | 8 | 42753056 | 3 prime UTR variant | G/C | snv | 0.39 | 2 | ||||
rs7812298 | 8 | 42753436 | intron variant | C/T | snv | 0.36 | 2 | ||||
rs7828365 | 8 | 42774171 | intron variant | C/T | snv | 0.14 | 2 | ||||
rs7178176 | 15 | 32151612 | intron variant | C/T | snv | 0.18 | 2 | ||||
rs755204 | 20 | 63362813 | intron variant | G/A | snv | 8.6E-02 | 2 |