Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs58982919 | 0.790 | 0.080 | 8 | 24956223 | missense variant | T/C | snv | 10 | |||
rs121908217 | 0.851 | 0.120 | 19 | 13308452 | missense variant | C/T | snv | 4.0E-06 | 9 | ||
rs11538758 | 0.882 | 0.160 | 20 | 4699534 | missense variant | C/A;T | snv | 8 | |||
rs138249161 | 0.827 | 0.240 | 12 | 106432421 | missense variant | T/A | snv | 2.7E-04 | 3.0E-04 | 8 | |
rs28933383 | 0.851 | 0.120 | 12 | 4912055 | missense variant | C/A;G;T | snv | 8 | |||
rs120074125 | 0.882 | 0.160 | 11 | 6393301 | missense variant | T/G | snv | 4.0E-06 | 7 | ||
rs121918544 | 0.827 | 0.200 | 14 | 24240635 | missense variant | C/T | snv | 7 | |||
rs672601362 | 0.851 | 0.080 | 2 | 240789246 | missense variant | G/A | snv | 7 | |||
rs74315402 | 0.882 | 0.200 | 20 | 4699570 | missense variant | C/T | snv | 7 | |||
rs755221106 | 0.851 | 0.040 | 17 | 50617560 | missense variant | G/A;T | snv | 4.0E-06 | 7 | ||
rs104894107 | 0.882 | 0.160 | 9 | 69064942 | missense variant | G/C;T | snv | 3.6E-05; 2.8E-05 | 6 | ||
rs137852763 | 0.851 | 0.320 | 11 | 94476318 | missense variant | C/G | snv | 6 | |||
rs2307441 | 0.882 | 0.080 | 15 | 89318595 | missense variant | T/C | snv | 2.9E-02 | 2.7E-02 | 6 | |
rs886041761 | 0.925 | 0.200 | 1 | 110603902 | missense variant | C/T | snv | 6 | |||
rs121908230 | 0.882 | 0.080 | 19 | 13262789 | missense variant | C/T | snv | 5 | |||
rs267606695 | 1.000 | 0.160 | 8 | 60266044 | missense variant | A/C;G | snv | 5 | |||
rs58332872 | 0.882 | 0.080 | 8 | 24956248 | missense variant | C/T | snv | 5 | |||
rs587777343 | 0.925 | 0.120 | 16 | 682232 | missense variant | C/T | snv | 5 | |||
rs104894699 | 0.925 | 0.120 | 19 | 50323694 | missense variant | C/T | snv | 4 | |||
rs121918514 | 0.925 | 0.080 | 19 | 53889705 | missense variant | G/A | snv | 4 | |||
rs1269252748 | 9 | 2641436 | missense variant | C/T | snv | 4 | |||||
rs28933381 | 0.925 | 0.080 | 12 | 4912102 | missense variant | G/C | snv | 4 | |||
rs730882234 | 0.925 | 17 | 59697725 | missense variant | T/G | snv | 4 | ||||
rs1057518988 | 0.925 | 0.040 | 12 | 13571859 | missense variant | T/C | snv | 3 | |||
rs118204095 | 1.000 | 0.160 | 11 | 119091414 | missense variant | G/A;T | snv | 4.5E-05 | 3 |