Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3077 | 0.701 | 0.440 | 6 | 33065245 | 3 prime UTR variant | A/G | snv | 0.29 | 16 | ||
rs1141718 | 0.724 | 0.280 | 6 | 159688224 | missense variant | A/G | snv | 15 | |||
rs4636297 | 0.724 | 0.360 | 9 | 136670698 | intron variant | A/G | snv | 0.67 | 0.65 | 14 | |
rs9277535 | 0.724 | 0.440 | 6 | 33087084 | 3 prime UTR variant | A/G | snv | 0.25 | 13 | ||
rs8067378 | 0.752 | 0.240 | 17 | 39895095 | regulatory region variant | A/G | snv | 0.50 | 12 | ||
rs3741219 | 0.776 | 0.280 | 11 | 1995389 | non coding transcript exon variant | A/G | snv | 0.42 | 10 | ||
rs1049216 | 0.790 | 0.200 | 4 | 184628935 | 3 prime UTR variant | A/G | snv | 0.27 | 9 | ||
rs11064 | 0.807 | 0.120 | 5 | 119393693 | 3 prime UTR variant | A/G | snv | 0.27 | 9 | ||
rs1834306 | 0.776 | 0.200 | 11 | 122152479 | intron variant | A/G | snv | 0.49 | 9 | ||
rs3087386 | 0.790 | 0.160 | 2 | 99439044 | missense variant | A/G | snv | 0.58 | 0.61 | 8 | |
rs4986764 | 0.827 | 0.120 | 17 | 61685986 | missense variant | A/G | snv | 0.60 | 0.61 | 8 | |
rs4851527 | 0.790 | 0.160 | 2 | 102005914 | intron variant | A/G | snv | 0.63 | 7 | ||
rs4579555 | 0.882 | 0.080 | 8 | 116867092 | intron variant | A/G | snv | 4 | |||
rs1030389 | 0.882 | 0.080 | 15 | 25032641 | non coding transcript exon variant | A/G | snv | 0.41 | 3 | ||
rs16945692 | 0.882 | 0.080 | 17 | 61862883 | intron variant | A/G | snv | 0.17 | 3 | ||
rs2862833 | 0.882 | 0.080 | 10 | 89015872 | 3 prime UTR variant | A/G | snv | 0.45 | 3 | ||
rs59661306 | 1.000 | 0.080 | 5 | 91087644 | intron variant | A/G | snv | 0.18 | 1 | ||
rs6547598 | 1.000 | 0.080 | 2 | 85219363 | intron variant | A/G | snv | 0.26 | 1 | ||
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs231775 | 0.504 | 0.720 | 2 | 203867991 | missense variant | A/G;T | snv | 0.42; 4.0E-06 | 115 | ||
rs5275 | 0.583 | 0.560 | 1 | 186673926 | 3 prime UTR variant | A/G;T | snv | 55 | |||
rs4646903 | 0.630 | 0.640 | 15 | 74719300 | downstream gene variant | A/G;T | snv | 0.18 | 36 | ||
rs1136201 | 0.645 | 0.280 | 17 | 39723335 | missense variant | A/G;T | snv | 0.20 | 34 | ||
rs1800624 | 0.658 | 0.480 | 6 | 32184610 | upstream gene variant | A/G;T | snv | 33 | |||
rs2844511 | 0.807 | 0.200 | 6 | 31422007 | intron variant | A/G;T | snv | 10 |