Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4986791 | 0.456 | 0.840 | 9 | 117713324 | missense variant | C/T | snv | 5.7E-02 | 4.9E-02 | 182 | |
rs2297518 | 0.658 | 0.480 | 17 | 27769571 | missense variant | G/A | snv | 0.18 | 0.17 | 30 | |
rs1130233 | 0.742 | 0.480 | 14 | 104773557 | synonymous variant | C/T | snv | 0.30 | 0.23 | 13 | |
rs10983755 | 0.790 | 0.320 | 9 | 117702392 | upstream gene variant | G/A | snv | 3.2E-02 | 7 | ||
rs12229892 | 0.807 | 0.240 | 12 | 112485589 | intron variant | G/A | snv | 1.4E-02 | 6 | ||
rs11536878 | 0.827 | 0.240 | 9 | 117709275 | intron variant | C/A | snv | 9.5E-02 | 5 | ||
rs158572 | 0.851 | 0.120 | 5 | 60943616 | intron variant | G/A | snv | 0.63 | 4 | ||
rs1917799 | 0.851 | 0.120 | 10 | 49542929 | upstream gene variant | A/C | snv | 0.25 | 4 | ||
rs2301756 | 0.851 | 0.120 | 12 | 112452972 | intron variant | A/G | snv | 0.21 | 4 | ||
rs3805246 | 0.882 | 0.120 | 4 | 143382955 | intron variant | G/A | snv | 0.31 | 3 | ||
rs6912200 | 0.925 | 0.080 | 6 | 41750170 | intron variant | C/T | snv | 0.54 | 3 |