Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 8
rs10224210 1.000 0.040 7 151716108 intron variant T/C snv 0.21 8
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8