Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3749147 | 0.882 | 0.120 | 2 | 27629051 | missense variant | G/A | snv | 0.23 | 0.20 | 6 | |
rs4665963 | 0.925 | 0.120 | 2 | 27305824 | splice region variant | T/C | snv | 0.35 | 0.43 | 3 | |
rs714052 | 0.925 | 0.120 | 7 | 73450539 | intron variant | A/G | snv | 9.2E-02 | 4 | ||
rs7586601 | 0.925 | 0.120 | 2 | 27361799 | intron variant | A/G | snv | 0.54 | 3 | ||
rs780090 | 0.925 | 0.120 | 2 | 27495607 | upstream gene variant | T/C;G | snv | 4 | |||
rs780092 | 0.827 | 0.160 | 2 | 27520287 | intron variant | A/G | snv | 0.18 | 5 | ||
rs780093 | 0.763 | 0.240 | 2 | 27519736 | intron variant | T/C | snv | 0.68 | 13 | ||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 24 | ||
rs7800944 | 0.882 | 0.160 | 7 | 73621527 | intron variant | T/C | snv | 0.28 | 4 | ||
rs799166 | 0.925 | 0.120 | 7 | 73637602 | intergenic variant | C/G | snv | 0.16 | 4 | ||
rs813592 | 0.925 | 0.120 | 2 | 27499104 | intron variant | T/C | snv | 0.42 | 0.47 | 3 | |
rs814295 | 0.925 | 0.120 | 2 | 27520348 | intron variant | A/G | snv | 0.18 | 5 |