Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12951053 0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs2078486 0.882 0.080 17 7679765 intron variant G/A;C snv 3
rs1429743956 0.882 0.080 17 7674906 stop gained T/A;C snv 3
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 56
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs1057520001 0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 23
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 21
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 19
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs1800371 0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs375275361 0.827 0.120 17 7675054 missense variant A/G;T snv 1.2E-05; 4.0E-06 5
rs587782596 0.807 0.200 17 7675071 missense variant G/A;T snv 5
rs1019340046 0.882 0.080 17 7674225 missense variant C/T snv 4
rs267605076 0.851 0.160 17 7674859 missense variant C/A;T snv 4.0E-06 4
rs1057519984 0.882 0.080 17 7673777 missense variant G/C;T snv 3
rs375573770 0.882 0.080 17 7670682 missense variant C/G snv 7.0E-06 3
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 3
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 3
rs587782769 0.882 0.080 17 7676155 missense variant G/A;C;T snv 1.6E-05; 1.2E-05; 4.0E-06 3
rs863224682 1.000 0.080 17 7669655 missense variant C/A;T snv 4.0E-06 2