Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9303521 0.925 0.120 17 45727828 intron variant T/C;G snv 0.60 5
rs12938031 0.851 0.160 17 45777136 intron variant A/G snv 0.26 4
rs1724422 1.000 0.040 17 45699947 intron variant A/G snv 0.47 2
rs34186148 1.000 0.040 17 45777289 intron variant G/A;C snv 0.31 2
rs35909029 1.000 0.040 17 45774132 intron variant T/A;C;G snv 2
rs62057061 1.000 0.040 17 45779273 intron variant C/G snv 0.14 2
rs7225384 1.000 0.040 17 45731730 non coding transcript exon variant C/G snv 0.39 2