Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs11752643 | 0.925 | 0.120 | 6 | 32701596 | downstream gene variant | C/T | snv | 2.3E-02 | 2 | ||
rs154972 | 0.925 | 0.120 | 6 | 32932874 | downstream gene variant | A/G | snv | 0.35 | 2 | ||
rs12663103 | 0.851 | 0.240 | 6 | 32193547 | intron variant | T/C | snv | 6.1E-02 | 7 | ||
rs3130215 | 0.882 | 0.240 | 6 | 33107186 | intron variant | A/G | snv | 0.69 | 3 | ||
rs423639 | 0.882 | 0.240 | 6 | 33019997 | intergenic variant | C/T | snv | 0.11 | 3 | ||
rs9276991 | 0.882 | 0.240 | 6 | 33014071 | upstream gene variant | A/G | snv | 6.0E-02 | 3 | ||
rs2395174 | 0.827 | 0.320 | 6 | 32437101 | upstream gene variant | T/G | snv | 0.24 | 5 | ||
rs204999 | 0.763 | 0.480 | 6 | 32142202 | intergenic variant | A/G | snv | 0.28 | 12 | ||
rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 7 | |
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 10 |