Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs3099844 0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 13
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10