Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs6903608 0.742 0.400 6 32460508 intron variant C/G;T snv 11
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 10
rs2734986 0.827 0.160 6 29850791 intron variant T/C snv 0.10 5
rs27524 0.851 0.160 5 96766240 intron variant A/G snv 0.61 4
rs6904029 0.851 0.200 6 29975290 non coding transcript exon variant G/A snv 0.29 0.26 4
rs10813831 0.925 0.120 9 32526148 missense variant G/A snv 0.21 0.24 2
rs6457715 0.925 0.120 6 33115411 intron variant A/G snv 0.35 2