Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1403934301 0.882 0.120 17 7631317 missense variant G/A snv 3
rs2518136 0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs7895340 0.851 0.160 10 113041766 intron variant G/A snv 0.53 4
rs2144908 0.851 0.120 20 44357077 intron variant G/A snv 0.18 5
rs9289231 0.827 0.120 3 124055231 intergenic variant T/G snv 0.15 5
rs6495446 0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs16933090 0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs1282382243 0.807 0.120 13 50843630 missense variant G/A snv 8
rs46522 0.807 0.120 17 48911235 non coding transcript exon variant C/T snv 0.40 8
rs198389 0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs20551 0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs1862513 0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs4754 0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs773641005 0.742 0.240 16 58723829 missense variant T/C snv 14
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs116843064 0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs1022113606 0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17