Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1049281 1.000 0.120 6 31268790 3 prime UTR variant T/C snv 0.68 3
rs10494360 1.000 0.120 1 161505960 non coding transcript exon variant G/A snv 0.10 9.0E-02 1
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs1050152 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 10
rs1050501 0.732 0.440 1 161674008 missense variant T/C snv 0.16 0.19 15
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051336 0.925 0.120 6 32444815 3 prime UTR variant G/A;C snv 0.15 2
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs1051792 0.851 0.240 6 31411200 missense variant G/A snv 0.34 0.35 5
rs1051794 0.925 0.120 6 31411332 missense variant G/A snv 0.34 0.35 5
rs10520789 1.000 0.120 15 95598638 regulatory region variant G/A snv 0.12 1
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1052248 1.000 0.120 6 31588804 3 prime UTR variant T/A snv 0.26 1
rs1055311 1.000 0.120 21 44289685 synonymous variant C/G;T snv 2.0E-05; 0.23 1
rs1055569 0.882 0.240 6 31472305 non coding transcript exon variant C/T snv 0.41 3
rs1057523354 0.763 0.480 13 110179387 missense variant C/A snv 13
rs1058587 0.882 0.200 19 18388612 missense variant C/G;T snv 0.24; 9.1E-06 4
rs1059288 0.882 0.320 6 33299895 3 prime UTR variant A/G snv 0.60 3
rs1059702 0.807 0.280 X 154018741 missense variant A/G snv 0.72 7
rs1059703 0.851 0.280 X 154013378 missense variant G/A snv 0.67 6
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs1063355 0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56 5
rs1063539 0.827 0.360 3 186857603 3 prime UTR variant G/A;C snv 0.10 5