Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs63750687 | 0.752 | 0.200 | 14 | 73217137 | missense variant | C/A;G;T | snv | 33 | |||
rs63750231 | 0.689 | 0.160 | 14 | 73198100 | missense variant | A/C;G | snv | 23 | |||
rs63750264 | 0.716 | 0.360 | 21 | 25891784 | missense variant | C/A;G;T | snv | 17 | |||
rs63750306 | 0.701 | 0.320 | 14 | 73173663 | missense variant | A/C;G;T | snv | 17 | |||
rs63750082 | 0.732 | 0.120 | 14 | 73192712 | missense variant | G/C;T | snv | 8.0E-06 | 13 | ||
rs63750083 | 0.732 | 0.160 | 14 | 73219177 | missense variant | C/A;T | snv | 13 | |||
rs63751287 | 0.742 | 0.120 | 14 | 73192792 | missense variant | A/G;T | snv | 13 | |||
rs63750522 | 0.827 | 0.120 | 14 | 73173644 | missense variant | G/A;C | snv | 8 | |||
rs63750577 | 0.827 | 0.120 | 14 | 73186881 | missense variant | C/T | snv | 8 | |||
rs63750852 | 0.790 | 0.120 | 14 | 73170998 | missense variant | G/A;T | snv | 8 | |||
rs63749806 | 0.827 | 0.080 | 14 | 73186902 | missense variant | T/C | snv | 7 | |||
rs63750599 | 0.827 | 0.160 | 14 | 73170963 | missense variant | T/C | snv | 7 | |||
rs63751037 | 0.790 | 0.080 | 14 | 73173642 | missense variant | A/G | snv | 7 | |||
rs63750646 | 0.807 | 0.120 | 14 | 73217147 | missense variant | G/C | snv | 6 | |||
rs63750730 | 0.827 | 0.120 | 14 | 73173574 | missense variant | C/T | snv | 6 | |||
rs63751235 | 0.807 | 0.120 | 14 | 73198117 | missense variant | C/G | snv | 6 | |||
rs533813519 | 0.851 | 0.120 | 1 | 226888097 | missense variant | C/A | snv | 1.9E-04 | 4.2E-05 | 5 | |
rs63749835 | 0.851 | 0.080 | 14 | 73192799 | missense variant | T/C | snv | 5 | |||
rs63749891 | 0.851 | 0.080 | 14 | 73198094 | missense variant | G/C;T | snv | 5 | |||
rs63750009 | 0.851 | 0.120 | 14 | 73192760 | missense variant | A/C;G | snv | 5 | |||
rs63751106 | 0.827 | 0.080 | 14 | 73173643 | missense variant | T/A;C | snv | 5 | |||
rs63751210 | 0.882 | 0.080 | 14 | 73186878 | missense variant | C/T | snv | 5 | |||
rs63750929 | 0.882 | 0.080 | 14 | 73217177 | missense variant | G/T | snv | 4 | |||
rs63751254 | 0.851 | 0.160 | 14 | 73217210 | missense variant | A/G | snv | 4 | |||
rs121917808 | 0.882 | 0.080 | 14 | 73219192 | missense variant | C/A | snv | 3 |