Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2921604 | 5 | 14867839 | intron variant | T/C | snv | 0.46 | 2 | ||||
rs2187668 | 0.701 | 0.480 | 6 | 32638107 | intron variant | C/T | snv | 3.3E-03 | 20 | ||
rs9271366 | 0.807 | 0.240 | 6 | 32619077 | intergenic variant | G/A | snv | 0.86 | 9 | ||
rs14399 | 6 | 111222741 | 3 prime UTR variant | C/A | snv | 0.32 | 3 | ||||
rs10265221 | 7 | 151717243 | intron variant | T/A;C | snv | 3 | |||||
rs878521 | 7 | 44216044 | downstream gene variant | G/A | snv | 0.33 | 3 | ||||
rs34642455 | 7 | 99777087 | intron variant | T/C | snv | 8.8E-03 | 1 | ||||
rs73359750 | 7 | 75848924 | intron variant | C/T | snv | 0.14 | 1 | ||||
rs2169387 | 8 | 9323885 | intron variant | A/G | snv | 0.87 | 6 | ||||
rs74331971 | 8 | 482881 | downstream gene variant | G/A | snv | 1.7E-02 | 2 | ||||
rs28491433 | 8 | 16193362 | intron variant | C/G | snv | 0.19 | 1 | ||||
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 34 | |||
rs579459 | 0.752 | 0.320 | 9 | 133278724 | upstream gene variant | C/T | snv | 0.81 | 28 | ||
rs495828 | 0.827 | 0.200 | 9 | 133279294 | upstream gene variant | T/G | snv | 0.81 | 24 | ||
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 22 | |||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 22 | |||
rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 18 | |||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 15 | |||
rs529565 | 0.851 | 0.120 | 9 | 133274084 | intron variant | C/T | snv | 13 | |||
rs514659 | 0.882 | 0.120 | 9 | 133266790 | intron variant | C/A;T | snv | 10 | |||
rs612169 | 9 | 133268030 | intron variant | G/A | snv | 10 | |||||
rs649129 | 1.000 | 0.080 | 9 | 133278860 | upstream gene variant | T/C;G | snv | 10 | |||
rs630014 | 9 | 133274306 | intron variant | G/A;C | snv | 9 | |||||
rs8176693 | 0.851 | 0.160 | 9 | 133262254 | intron variant | C/T | snv | 9.9E-02 | 9 | ||
rs545971 | 9 | 133267960 | intron variant | T/A;C | snv | 8 |