Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7195386 | 0.925 | 0.120 | 16 | 24567137 | splice region variant | T/A;C | snv | 0.56 | 2 | ||
rs72755233 | 1.000 | 0.080 | 15 | 100152748 | missense variant | G/A;T | snv | 7.1E-02; 3.2E-05 | 5 | ||
rs7534091 | 1 | 118321993 | intergenic variant | A/G | snv | 0.23 | 2 | ||||
rs76895963 | 1.000 | 0.080 | 12 | 4275678 | intron variant | T/G | snv | 1.5E-02 | 6 | ||
rs76929617 | 12 | 120429995 | intergenic variant | A/G | snv | 3.7E-02 | 2 | ||||
rs7740107 | 1.000 | 0.080 | 6 | 130053316 | intron variant | T/A;G | snv | 6 | |||
rs780094 | 0.658 | 0.400 | 2 | 27518370 | intron variant | T/C | snv | 0.67 | 35 | ||
rs7826312 | 8 | 32542597 | intron variant | T/C | snv | 0.57 | 2 | ||||
rs9880211 | 3 | 136388707 | intron variant | G/A | snv | 0.19 | 2 |