Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs429358 | 0.590 | 0.600 | 19 | 44908684 | missense variant | T/C | snv | 0.14 | 0.16 | 26 | |
rs10033900 | 0.807 | 0.040 | 4 | 109737911 | intron variant | T/C | snv | 0.54 | 5 | ||
rs1061170 | 0.561 | 0.720 | 1 | 196690107 | missense variant | C/T | snv | 0.68 | 0.64 | 5 | |
rs11080055 | 0.851 | 0.040 | 17 | 28322698 | intron variant | A/C | snv | 0.54 | 5 | ||
rs1410996 | 0.807 | 0.240 | 1 | 196727803 | intron variant | G/A | snv | 0.46 | 5 | ||
rs570618 | 0.827 | 0.040 | 1 | 196687934 | intron variant | T/G | snv | 0.69 | 5 | ||
rs62358361 | 0.851 | 0.040 | 5 | 39327786 | intron variant | G/C;T | snv | 5 | |||
rs72802342 | 0.851 | 0.040 | 16 | 75200974 | downstream gene variant | C/A | snv | 6.2E-02 | 5 | ||
rs1831282 | 1.000 | 0.040 | 1 | 196704863 | intron variant | A/C | snv | 0.62 | 2 |