Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 25 | |
rs579459 | 0.752 | 0.320 | 9 | 133278724 | upstream gene variant | C/T | snv | 0.81 | 17 | ||
rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 14 | |||
rs505922 | 0.689 | 0.520 | 9 | 133273813 | intron variant | C/T | snv | 12 | |||
rs612169 | 9 | 133268030 | intron variant | G/A | snv | 10 | |||||
rs2187668 | 0.701 | 0.480 | 6 | 32638107 | intron variant | C/T | snv | 3.3E-03 | 10 | ||
rs630014 | 9 | 133274306 | intron variant | G/A;C | snv | 9 | |||||
rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 9 | |||
rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 9 | |||
rs495828 | 0.827 | 0.200 | 9 | 133279294 | upstream gene variant | T/G | snv | 0.81 | 8 | ||
rs649129 | 1.000 | 0.080 | 9 | 133278860 | upstream gene variant | T/C;G | snv | 8 | |||
rs9271366 | 0.807 | 0.240 | 6 | 32619077 | intergenic variant | G/A | snv | 0.86 | 8 | ||
rs514659 | 0.882 | 0.120 | 9 | 133266790 | intron variant | C/A;T | snv | 8 | |||
rs529565 | 0.851 | 0.120 | 9 | 133274084 | intron variant | C/T | snv | 8 | |||
rs545971 | 9 | 133267960 | intron variant | T/A;C | snv | 8 | |||||
rs674302 | 9 | 133271249 | intron variant | A/T | snv | 8 | |||||
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 8 | |
rs635634 | 0.882 | 0.160 | 9 | 133279427 | upstream gene variant | T/A;C | snv | 7 | |||
rs643434 | 9 | 133266942 | intron variant | A/G;T | snv | 7 | |||||
rs644234 | 9 | 133266804 | intron variant | G/T | snv | 7 | |||||
rs560887 | 0.827 | 0.120 | 2 | 168906638 | intron variant | T/C | snv | 0.79 | 0.80 | 7 | |
rs8176693 | 0.851 | 0.160 | 9 | 133262254 | intron variant | C/T | snv | 9.9E-02 | 5 | ||
rs2657879 | 1.000 | 0.080 | 12 | 56471554 | missense variant | A/G | snv | 0.17 | 0.15 | 5 | |
rs514708 | 9 | 133258352 | intron variant | C/T | snv | 0.29 | 4 | ||||
rs626035 | 9 | 133259603 | intron variant | T/G | snv | 0.28 | 4 |