Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1003878 0.882 0.200 6 32332045 stop gained G/A snv 0.19 0.23 3
rs1003879 1.000 0.120 6 32331815 intron variant G/A snv 0.41 1
rs1004819 0.776 0.360 1 67204530 intron variant G/A snv 0.30 1
rs10168266 0.776 0.400 2 191071078 intron variant C/T snv 0.19 3
rs10174238 0.724 0.200 2 191108308 intron variant G/A snv 0.70 1
rs10175798 1.000 0.120 2 30226728 upstream gene variant G/A snv 0.51 1
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs1018430 1.000 0.120 6 32313911 intron variant C/T snv 0.25 1
rs1018431 1.000 0.120 6 32313899 intron variant G/A snv 0.25 1
rs1018433 1.000 0.120 6 32313733 intron variant A/T snv 0.21 1
rs1018434 1.000 0.120 6 32313583 intron variant T/C snv 0.21 1
rs10209110 1.000 0.120 2 100056230 intron variant C/T snv 0.47 1
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs1033500 1.000 0.120 6 32339605 missense variant G/A snv 0.40 0.33 2
rs1034323 1.000 0.120 6 30400858 intergenic variant C/T snv 0.43 1
rs1035142 0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 1
rs1041885 1.000 0.120 6 32445032 3 prime UTR variant T/A snv 0.15 1
rs1042127 0.925 0.120 6 31116393 missense variant A/C snv 0.21 0.17 1
rs1042337 1.000 0.120 6 32937204 missense variant G/A snv 0.78 0.80 1
rs1042448 1.000 0.120 6 33086565 3 prime UTR variant T/A;C snv 6.1E-03; 7.4E-06 1
rs1042544 0.925 0.200 6 33086680 3 prime UTR variant A/G snv 0.38 2
rs1042663 0.925 0.160 6 31937353 synonymous variant G/A snv 9.7E-02 0.12 2
rs1043099 1.000 0.120 22 30285268 3 prime UTR variant C/A;G;T snv 1
rs1046080 1.000 0.120 6 31628105 missense variant C/A snv 0.79 0.74 1
rs10484544 1.000 0.120 6 29027942 upstream gene variant T/C snv 0.22 1