Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174577 1.000 0.080 11 61837342 intron variant C/A snv 0.38 13
rs174545 1.000 0.080 11 61801834 3 prime UTR variant C/A;G snv 0.28 5
rs174528 1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs2581624 3 142915027 intron variant G/C;T snv 0.29 2