Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs344781 0.807 0.200 19 43670636 upstream gene variant C/T snv 0.80 7
rs10744676 0.925 0.080 12 5043783 upstream gene variant C/T snv 0.88 2