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
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs16910526 0.742 0.280 12 10118488 stop gained A/C;G snv 6.2E-02 12
rs2296135 0.851 0.080 10 5952731 3 prime UTR variant A/C snv 0.58 5
rs1059293 0.882 0.080 21 33437386 3 prime UTR variant C/T snv 0.59 3