Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9825420 0.851 0.080 3 37562521 intron variant T/G snv 0.18 4
rs10029851 0.851 0.080 4 108706869 intergenic variant A/C;T snv 4
rs11590421 0.851 0.080 1 38528443 intergenic variant G/A snv 0.15 4
rs1559473 0.851 0.080 2 222016799 intergenic variant T/G snv 0.25 4
rs1605070 0.851 0.080 3 51882999 intergenic variant C/A snv 0.60 4
rs16938145 0.851 0.080 9 2256092 intergenic variant T/C;G snv 4
rs2322978 0.851 0.080 11 127846245 intergenic variant A/G snv 0.74 4
rs2457174 0.851 0.080 5 133843389 intergenic variant C/T snv 0.33 4
rs2685056 0.851 0.080 3 104699729 intergenic variant G/A snv 0.50 4
rs4424056 0.851 0.080 6 91135689 intergenic variant T/G snv 0.76 4
rs551585 0.851 0.080 1 76660688 intergenic variant C/A snv 8.9E-02 4
rs72911847 0.851 0.080 2 193714051 intergenic variant A/G snv 3.3E-02 4
rs730547 0.851 0.080 17 34785087 intergenic variant C/T snv 0.20 4
rs75285952 0.851 0.080 4 27902934 intergenic variant G/A snv 3.3E-02 4
rs9327881 0.851 0.080 5 103389394 intergenic variant G/A snv 0.13 4
rs9329300 0.851 0.080 10 2747402 intergenic variant A/C;G snv 4
rs9977018 0.851 0.080 21 41616809 intergenic variant T/G snv 0.24 4
rs11987758 0.851 0.080 8 2180583 regulatory region variant G/A snv 0.12 4
rs4761659 0.851 0.080 12 93293308 regulatory region variant T/C snv 0.89 4
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs74315452 0.732 0.160 21 31667356 missense variant T/C snv 12
rs80265967 0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs1002442 0.851 0.080 10 60043304 non coding transcript exon variant T/G snv 0.14 4
rs3849942 0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs3849943 0.827 0.080 9 27543384 non coding transcript exon variant C/G;T snv 5