Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs12150660 1.000 0.040 17 7618597 intron variant G/T snv 0.17 5
rs6258 1.000 0.040 17 7631360 missense variant C/A;T snv 5.6E-05; 4.5E-03 5
rs2075230 17 7583790 5 prime UTR variant A/C;G snv 4.0E-06; 0.19 3