Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs72645347 | 0.790 | 0.280 | 17 | 50196337 | missense variant | G/A | snv | 10 | |||
rs72653170 | 0.752 | 0.240 | 17 | 50188908 | missense variant | G/A | snv | 8.0E-06 | 10 | ||
rs67682641 | 0.807 | 0.240 | 17 | 50194375 | missense variant | C/A;T | snv | 6 | |||
rs28937869 | 0.851 | 0.200 | 5 | 177608994 | missense variant | C/T | snv | 4.8E-05 | 9.1E-05 | 4 | |
rs72654799 | 0.882 | 0.200 | 17 | 50188541 | missense variant | G/A;C | snv | 6.4E-05 | 3 | ||
rs61735045 | 0.882 | 0.160 | 9 | 134750808 | missense variant | G/A | snv | 3.5E-02 | 3.1E-02 | 3 | |
rs137853315 | 0.882 | 0.200 | X | 154368081 | missense variant | G/A | snv | 3 | |||
rs72648365 | 0.925 | 0.240 | 17 | 50193990 | missense variant | G/A;C | snv | 2 | |||
rs72656307 | 0.925 | 0.240 | 17 | 50187968 | missense variant | G/A | snv | 2.4E-05 | 2.1E-05 | 2 | |
rs886440452 | 0.925 | 0.200 | 17 | 50189478 | missense variant | G/A | snv | 4.0E-06 | 2.8E-05 | 2 | |
rs1186920009 | 0.925 | 0.200 | 7 | 94427227 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
rs863223491 | 0.925 | 0.160 | 2 | 189062865 | splice region variant | C/T | snv | 2 | |||
rs121912932 | 0.925 | 0.160 | 9 | 134820135 | missense variant | G/A | snv | 2 | |||
rs780400029 | 0.925 | 0.200 | 9 | 134835169 | missense variant | A/G | snv | 1.6E-04 | 3.5E-05 | 2 |