Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs7848647 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 6
rs4979462 0.790 0.240 9 114804733 intron variant C/T snv 0.13 2
rs6478109 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 2
rs3810936 0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 1
rs4263839 0.807 0.160 9 114804160 intron variant A/G snv 0.75 1
rs6478108 0.763 0.200 9 114796423 intron variant C/T snv 0.73 1