Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587782144 0.807 0.160 17 7675139 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 5
rs587782596 0.807 0.200 17 7675071 missense variant G/A;T snv 5
rs779196500 0.882 0.120 17 7675187 missense variant G/A snv 4.0E-06 5
rs2287499 0.925 0.080 17 7688850 missense variant C/G;T snv 0.20 4
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 4
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 4
rs1064795369 0.882 0.080 17 7673791 missense variant A/C;G snv 3
rs1159579789 0.925 0.080 17 7673578 missense variant T/C snv 4.0E-06 3
rs372201428 0.882 0.120 17 7676181 missense variant G/A;C snv 1.2E-05 3
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 2
rs1057520006 0.752 0.240 17 7673799 missense variant A/C;G;T snv 2
rs1064794312 0.925 0.080 17 7674278 missense variant A/G snv 8.0E-06 2
rs1177881399 0.925 0.080 17 7673557 missense variant T/C snv 4.0E-06 2
rs1237722021 0.925 0.080 17 7676194 missense variant C/A snv 7.0E-06 2
rs587781433 0.925 0.080 17 7674197 missense variant T/C;G snv 2
rs587782646 0.925 0.080 17 7676576 missense variant C/G snv 4.0E-06 2
rs587782705 0.807 0.280 17 7675157 missense variant G/A snv 8.0E-06 2
rs876660825 1.000 0.080 17 7674962 missense variant G/A;C snv 1
rs1131691036 0.851 0.080 17 7675207 frameshift variant GCA/CC delins 7
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213