Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 | ||
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs121913254 | 0.658 | 0.440 | 1 | 114713909 | stop gained | G/A;C;T | snv | 31 | |||
rs121913238 | 0.732 | 0.240 | 12 | 25227343 | missense variant | G/C;T | snv | 17 | |||
rs121912520 | 0.851 | 0.240 | 2 | 48688020 | missense variant | C/G | snv | 4 | |||
rs746394859 | 0.882 | 0.120 | 11 | 35229182 | missense variant | A/G | snv | 4.0E-06 | 3 | ||
rs121912525 | 0.882 | 0.240 | 2 | 48687950 | missense variant | G/T | snv | 2.0E-05 | 4.9E-05 | 3 | |
rs121912523 | 0.925 | 0.240 | 2 | 48688162 | stop gained | G/T | snv | 8.0E-06 | 2 | ||
rs61755294 | 1.000 | 0.080 | 11 | 35221671 | missense variant | G/A;C | snv | 1.2E-05; 8.0E-06 | 1 | ||
rs12470652 | 1.000 | 0.080 | 2 | 48694299 | missense variant | T/C | snv | 3.8E-02 | 3.8E-02 | 1 | |
rs917607255 | 1.000 | 0.080 | 2 | 48755643 | missense variant | A/G | snv | 1 | |||
rs1183057432 | 1.000 | 0.080 | 3 | 12584570 | missense variant | T/C | snv | 4.0E-06 | 1 |