Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs555743307 0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs148704956 0.716 0.360 6 52187772 missense variant A/G snv 8.0E-06 7.0E-06 19
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 14
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 14
rs2076530 0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs33996649 0.732 0.400 1 113852067 missense variant C/T snv 1.7E-02 1.6E-02 13
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18