Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121913396 | 0.732 | 0.200 | 3 | 41224607 | missense variant | A/C;G;T | snv | 13 | |||
rs121913357 | 0.742 | 0.320 | 7 | 140781603 | stop gained | C/A;G;T | snv | 12 | |||
rs121913407 | 0.763 | 0.240 | 3 | 41224645 | missense variant | T/C;G | snv | 12 | |||
rs397516896 | 0.763 | 0.360 | 7 | 140753355 | missense variant | C/G;T | snv | 11 | |||
rs121913361 | 0.807 | 0.280 | 7 | 140753349 | missense variant | C/A;G;T | snv | 7 | |||
rs1057519732 | 0.827 | 0.160 | 15 | 66436824 | missense variant | C/A;T | snv | 6 | |||
rs397516792 | 0.827 | 0.280 | 15 | 66436825 | missense variant | C/A;G;T | snv | 6 |