Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs272888 1.000 0.040 5 132329730 intron variant T/C snv 0.71 1
rs1050152 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 1