Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs5743708 | 0.525 | 0.800 | 4 | 153705165 | missense variant | G/A | snv | 1.7E-02 | 1.8E-02 | 98 | |
rs621559 | 0.827 | 0.080 | 1 | 43179740 | intron variant | G/A | snv | 0.18 | 5 | ||
rs6489769 | 0.851 | 0.120 | 12 | 963799 | intron variant | C/A;T | snv | 4 | |||
rs662 | 0.485 | 0.840 | 7 | 95308134 | missense variant | T/C | snv | 0.38 | 0.42 | 157 | |
rs72554204 | 0.827 | 0.120 | 19 | 43546062 | missense variant | C/T | snv | 1.2E-04 | 1.3E-04 | 5 | |
rs7963551 | 0.807 | 0.160 | 12 | 912349 | 3 prime UTR variant | T/G | snv | 0.13 | 7 | ||
rs833061 | 0.605 | 0.600 | 6 | 43769749 | upstream gene variant | C/G;T | snv | 42 | |||
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 | |
rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
rs920778 | 0.633 | 0.480 | 12 | 53966448 | intron variant | G/A | snv | 0.57 | 36 | ||
rs9288516 | 0.827 | 0.120 | 2 | 216188541 | intron variant | T/A | snv | 5.0E-02 | 6 |