Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs12722495 0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 5
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2516509 0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs907715 0.752 0.520 4 122613898 intron variant C/T snv 0.35 11
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs12150220 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2304256 0.732 0.360 19 10364976 missense variant C/A snv 0.27 0.23 13
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs3733197 0.742 0.320 4 101918130 missense variant G/A snv 0.31 0.30 13
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36