Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs34557412 0.763 0.240 17 16948873 missense variant A/G snv 3.5E-03 3.9E-03 15
rs3731211 9 21986848 intron variant T/A snv 0.74 7
rs6475611 9 22151140 intergenic variant G/A snv 0.21 6
rs13063578 3 47046347 intron variant T/A snv 0.46 5