Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 14
rs121917737 0.827 0.080 10 79557264 missense variant C/A snv 5
rs121917738 0.827 0.080 10 79557363 missense variant A/G snv 5