Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs375869205 | 1.000 | 0.080 | 5 | 103003097 | missense variant | C/G;T | snv | 1 | |||
rs61761208 | 0.882 | 0.080 | 1 | 226885602 | missense variant | A/T | snv | 3 | |||
rs63750215 | 0.701 | 0.240 | 1 | 226885603 | missense variant | A/T | snv | 19 | |||
rs28936379 | 0.807 | 0.120 | 1 | 226888977 | missense variant | A/C;G;T | snv | 4.0E-06 | 10 | ||
rs63750264 | 0.716 | 0.360 | 21 | 25891784 | missense variant | C/A;G;T | snv | 17 | |||
rs1315025573 | 0.925 | 0.080 | 21 | 25891849 | missense variant | A/C;G | snv | 4.0E-06 | 2 | ||
rs63750847 | 0.790 | 0.120 | 21 | 25897620 | missense variant | C/T | snv | 4.5E-04 | 3.0E-04 | 8 | |
rs1038162399 | 0.925 | 0.080 | 21 | 25911954 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
rs1341026713 | 0.925 | 0.080 | 21 | 25955719 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 3 | |
rs201085152 | 0.925 | 0.080 | 21 | 25975072 | missense variant | G/A;T | snv | 1.6E-05; 3.6E-05 | 3 | ||
rs1451944248 | 0.925 | 0.080 | 21 | 25975964 | missense variant | G/A | snv | 2 | |||
rs1302192564 | 0.925 | 0.080 | 21 | 26000164 | missense variant | G/A | snv | 2 | |||
rs201093867 | 0.925 | 0.080 | 21 | 26021995 | missense variant | A/C | snv | 2 | |||
rs1200601649 | 0.925 | 0.080 | 21 | 26022022 | missense variant | A/C | snv | 2 | |||
rs1396086494 | 0.851 | 0.080 | 21 | 26051069 | missense variant | G/A | snv | 4.0E-06 | 6 | ||
rs1231783932 | 0.763 | 0.120 | 21 | 26051171 | missense variant | T/A;C | snv | 1.2E-05 | 11 | ||
rs63750424 | 0.677 | 0.240 | 17 | 46024061 | missense variant | C/T | snv | 1.6E-05 | 30 | ||
rs63750601 | 0.882 | 0.080 | 14 | 73170995 | missense variant | G/T | snv | 3 | |||
rs63751278 | 0.827 | 0.120 | 14 | 73173631 | missense variant | A/G | snv | 6 | |||
rs63751106 | 0.827 | 0.080 | 14 | 73173643 | missense variant | T/A;C | snv | 5 | |||
rs63750306 | 0.701 | 0.320 | 14 | 73173663 | missense variant | A/C;G;T | snv | 17 | |||
rs63749885 | 0.882 | 0.080 | 14 | 73186859 | missense variant | C/T | snv | 3 | |||
rs63750590 | 0.790 | 0.120 | 14 | 73186860 | missense variant | A/G | snv | 10 | |||
rs63749806 | 0.827 | 0.080 | 14 | 73186902 | missense variant | T/C | snv | 7 | |||
rs63750082 | 0.732 | 0.120 | 14 | 73192712 | missense variant | G/C;T | snv | 8.0E-06 | 13 |