Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs78378222 0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs760043106 0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1057520001 0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs483352697 0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs587781991 0.724 0.240 17 7675208 missense variant C/A;T snv 17
rs1800371 0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs12951053 0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs1625895 0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs587782596 0.807 0.200 17 7675071 missense variant G/A;T snv 7
rs1131691022 0.827 0.160 17 7670685 frameshift variant GG/A;G delins 6
rs267605076 0.851 0.160 17 7674859 missense variant C/A;T snv 4.0E-06 6
rs9895829 0.807 0.080 17 7675361 5 prime UTR variant A/G snv 7.4E-02 6
rs1019340046 0.882 0.080 17 7674225 missense variant C/T snv 5
rs2909430 0.827 0.200 17 7675327 5 prime UTR variant C/G;T snv 5
rs375275361 0.827 0.120 17 7675054 missense variant A/G;T snv 1.2E-05; 4.0E-06 5