Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28935468 0.732 0.240 X 154030912 missense variant G/A snv 17
rs6746030 0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs7439366 0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs885479 0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs74315431 0.732 0.080 20 58418318 missense variant C/T snv 4.0E-06 15
rs1042173 0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs121908552 0.763 0.160 17 63964587 missense variant C/A;G;T snv 4.0E-06 14
rs2069718 0.742 0.320 12 68156382 intron variant A/G;T snv 0.50 14
rs2241883 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs11674595 0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs2069840 0.742 0.360 7 22728953 intron variant C/G snv 0.27 13
rs1554781700 0.851 0.240 9 134701287 missense variant G/T snv 12
rs1200746244 0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs165774 0.807 0.120 22 19965038 3 prime UTR variant G/A snv 0.27 11
rs121913365 0.776 0.320 7 140753332 missense variant T/A;G snv 10
rs6269 0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs1834306 0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs208294 0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9
rs5277 0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 9
rs61748421 0.807 0.200 X 154031326 stop gained G/A;T snv 9
rs6267 0.827 0.200 22 19962740 missense variant G/A;T snv 4.8E-05; 1.4E-02 9
rs80338958 0.790 0.200 17 63945614 missense variant C/A;T snv 1.6E-05; 5.6E-05 9
rs1057518946 0.882 0.080 X 71223816 missense variant G/T snv 8
rs222747 0.827 0.240 17 3589906 missense variant C/A;G;T snv 0.72; 4.5E-06 8
rs3813034 0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8