Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
rs8099917 | 0.581 | 0.600 | 19 | 39252525 | upstream gene variant | T/G | snv | 0.16 | 60 | ||
rs855791 | 0.701 | 0.400 | 22 | 37066896 | missense variant | A/G;T | snv | 0.57; 4.0E-06 | 38 | ||
rs334 | 0.724 | 0.240 | 11 | 5227002 | missense variant | T/A;C;G | snv | 3.5E-03 | 35 | ||
rs72661131 | 0.742 | 0.480 | 10 | 52771739 | upstream gene variant | A/G | snv | 7.6E-04 | 15 | ||
rs9399137 | 0.851 | 0.320 | 6 | 135097880 | intron variant | T/C | snv | 0.20 | 13 | ||
rs104894809 | 0.790 | 0.120 | X | 48792371 | missense variant | G/A | snv | 9.5E-06 | 9 | ||
rs121912748 | 0.790 | 0.200 | 17 | 44253327 | missense variant | C/T | snv | 4.0E-05 | 2.1E-05 | 9 | |
rs33950507 | 0.807 | 0.080 | 11 | 5226943 | stop gained | C/A;G;T | snv | 2.5E-04 | 8 | ||
rs766432 | 0.925 | 0.080 | 2 | 60492835 | intron variant | C/A | snv | 0.80 | 6 | ||
rs766814208 | 0.851 | 0.120 | 10 | 95823259 | synonymous variant | C/T | snv | 1.6E-05 | 2.8E-05 | 5 | |
rs1283391088 | 0.882 | 0.120 | 16 | 176755 | synonymous variant | C/T | snv | 1.4E-05 | 4 | ||
rs186590045 | 16 | 31528549 | missense variant | T/G | snv | 1.0E-04 | 3.5E-05 | 1 | |||
rs387906544 | 16 | 177072 | missense variant | C/G | snv | 1 | |||||
rs41467944 | 16 | 172991 | missense variant | G/A | snv | 1 | |||||
rs368698783 | 11 | 5249833 | 5 prime UTR variant | C/T | snv | 0.15 | 1 | ||||
rs3760053 | 16 | 161244 | intron variant | T/C;G | snv | 1 |