Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs10274928 7 28102469 intron variant A/G;T snv 2