Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs12150220 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
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
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
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
rs2516398 0.882 0.200 6 31513749 upstream gene variant G/T snv 0.70 3
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
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs2844494 0.925 0.160 6 31515638 upstream gene variant C/A snv 0.70 2
rs2856705 0.882 0.200 6 32703179 downstream gene variant C/T snv 0.11 3
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193