Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52