Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799939 | 0.658 | 0.280 | 10 | 43114671 | missense variant | G/A;C;T | snv | 0.21 | 27 | ||
rs121909218 | 0.672 | 0.360 | 10 | 87933145 | missense variant | G/A | snv | 25 | |||
rs4939827 | 0.708 | 0.160 | 18 | 48927093 | intron variant | T/A;C | snv | 25 | |||
rs371769427 | 0.683 | 0.400 | 21 | 43104346 | missense variant | G/A;T | snv | 8.0E-06 | 24 | ||
rs75076352 | 0.689 | 0.240 | 10 | 43114500 | missense variant | T/A;C;G | snv | 1.2E-05 | 24 | ||
rs1801270 | 0.689 | 0.400 | 6 | 36684194 | missense variant | C/A;T | snv | 0.15; 4.4E-05 | 22 | ||
rs75996173 | 0.716 | 0.240 | 10 | 43114501 | missense variant | G/A;C;T | snv | 4.0E-06; 4.0E-06 | 21 | ||
rs121913412 | 0.724 | 0.280 | 3 | 41224633 | missense variant | A/C;G;T | snv | 19 | |||
rs11568818 | 0.763 | 0.280 | 11 | 102530930 | upstream gene variant | T/A;C | snv | 15 | |||
rs121918461 | 0.827 | 0.240 | 12 | 112450362 | missense variant | A/C;G;T | snv | 12 | |||
rs966423 | 0.776 | 0.200 | 2 | 217445617 | intron variant | C/G;T | snv | 11 | |||
rs3741219 | 0.776 | 0.280 | 11 | 1995389 | non coding transcript exon variant | A/G | snv | 0.42 | 10 | ||
rs1418810723 | 0.851 | 0.080 | 2 | 215409981 | missense variant | A/T | snv | 8.0E-06 | 9 | ||
rs1057519906 | 0.882 | 0.120 | 15 | 90088607 | missense variant | T/A;C | snv | 8 | |||
rs387906698 | 0.827 | 0.040 | 7 | 142751919 | missense variant | C/A;T | snv | 4.0E-06; 7.2E-05 | 8 | ||
rs4769793 | 0.807 | 0.120 | 13 | 29985289 | intergenic variant | G/C | snv | 8 | |||
rs763538721 | 0.807 | 0.160 | 14 | 61740897 | missense variant | T/A | snv | 4.0E-06 | 8 | ||
rs104894403 | 0.851 | 0.240 | 13 | 20189386 | missense variant | C/A;G;T | snv | 4.0E-06 | 7 | ||
rs12918952 | 0.851 | 0.120 | 16 | 78386878 | missense variant | G/A;C;T | snv | 7 | |||
rs737241 | 0.827 | 0.120 | 4 | 73451012 | intron variant | G/A;C | snv | 7 | |||
rs1057519788 | 0.925 | 0.080 | 6 | 117317184 | missense variant | C/T | snv | 6 | |||
rs1373481065 | 0.827 | 0.040 | 1 | 67687668 | missense variant | A/G | snv | 4.0E-06 | 6 | ||
rs3130 | 0.882 | 0.080 | 4 | 15968315 | 3 prime UTR variant | T/A;C | snv | 6 | |||
rs3829078 | 0.851 | 0.160 | 9 | 35679254 | missense variant | A/G;T | snv | 8.2E-02 | 6 | ||
rs80358829 | 0.827 | 0.120 | 13 | 32340327 | missense variant | C/T | snv | 6 |