Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912664 0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 40
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 20
rs372201428 0.882 0.120 17 7676181 missense variant G/A;C snv 1.2E-05 3
rs375275361 0.827 0.120 17 7675054 missense variant A/G;T snv 1.2E-05; 4.0E-06 5
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs587778718 1.000 0.080 17 7674959 missense variant G/A;C;T snv 4.0E-06; 1.2E-05; 4.0E-06 2
rs770374782 0.851 0.160 17 7673752 missense variant G/A;C snv 1.2E-05 4.2E-05 6
rs201744589 0.882 0.240 17 7673728 stop gained C/A;G;T snv 4.0E-06; 1.2E-05 3
rs730881997 0.925 0.200 17 7675999 missense variant A/C;T snv 8.0E-06 4
rs375338359 0.882 0.200 17 7670684 missense variant C/G;T snv 8.0E-06 2
rs758781593 17 7675204 missense variant T/A;C;G snv 8.0E-06 2
rs989692988 17 7676023 splice donor variant A/C snv 8.0E-06 1
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 56
rs587782705 0.807 0.280 17 7675157 missense variant G/A snv 8.0E-06 2
rs1060501206 17 7675056 missense variant C/T snv 8.0E-06 1
rs587780728 1.000 0.120 17 7676224 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 13
rs1064794312 0.925 0.080 17 7674278 missense variant A/G snv 8.0E-06 2
rs876660829 17 7673598 missense variant G/C;T snv 8.0E-06 2
rs750893877 0.807 0.320 17 7674258 synonymous variant G/A snv 8.0E-06 7
rs587780076 17 7673743 missense variant C/A;T snv 8.0E-06; 8.0E-06 1
rs781490101 0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06 5
rs1288373809 0.882 0.120 17 7673255 synonymous variant G/A snv 5.3E-06 5
rs768803947 0.882 0.080 17 7670624 missense variant C/A;T snv 4.0E-06; 4.0E-06 3
rs730882028 1.000 0.120 17 7670709 missense variant C/A;G;T snv 4.0E-06 2