Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs79105258 12 111280427 intron variant C/A;T snv 24
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs1407040 20 58897119 intron variant C/T snv 0.70 4