Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs1556425596 0.752 0.240 21 45989967 intron variant C/T snv 37
rs113871094 0.683 0.320 15 48465820 stop gained G/A snv 34
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1331463984 0.701 0.240 16 2176350 missense variant G/A snv 33
rs1563183492 0.708 0.520 7 70766248 missense variant C/T snv 32
rs80338945 0.695 0.440 13 20189313 missense variant A/G snv 6.4E-04 6.4E-04 32
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs398124401 0.695 0.480 4 55346393 stop gained G/A snv 1.2E-04 2.8E-05 25
rs148881970 0.724 0.360 17 42543840 missense variant A/G snv 5.4E-05 1.3E-04 22
rs1085307845 0.752 0.320 6 79025582 missense variant G/T snv 21
rs555145190 0.732 0.360 17 42543921 stop gained G/A;C;T snv 4.2E-06 21
rs587784105 0.732 0.440 5 177235863 stop gained G/A snv 19
rs765379963 0.701 0.520 1 165743172 stop gained G/A snv 1.2E-05 2.1E-05 19
rs61750240 0.752 0.240 X 154031020 stop gained G/A;C snv 5.5E-06 17
rs797044849 0.807 0.160 12 13567164 missense variant C/A;G;T snv 4.0E-06 17
rs28935468 0.732 0.240 X 154030912 missense variant G/A snv 14
rs1555740650 0.807 0.240 19 49596253 stop gained G/T snv 13
rs1568019012 0.790 0.360 18 6985616 stop gained G/A snv 13
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs1060499733 0.851 0.120 3 47846757 missense variant A/G snv 11
rs112795301 0.776 0.160 3 70972634 stop gained G/A snv 11
rs886041116 0.776 0.240 20 50892526 stop gained G/A snv 11
rs1064793345 0.752 0.240 10 87961039 missense variant T/C snv 10