Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs767685429 0.882 0.120 19 41332206 missense variant G/A;C snv 2.8E-05; 8.0E-06 3
rs2241716 1.000 0.080 19 41348181 intron variant C/T snv 4.0E-02 2