Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs759412116 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19