Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112846137 0.851 0.160 3 160595133 intergenic variant G/T snv 5.3E-02 4
rs1131012 0.763 0.280 17 64350416 missense variant T/C snv 0.38 10
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs1150753 0.925 0.120 6 32092090 intron variant A/G snv 6.3E-02 2
rs11568821 0.827 0.200 2 241851760 intron variant C/G;T snv 10
rs117026326 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 10
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1217393 0.851 0.160 1 113891324 intron variant G/A snv 0.42 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1234315 0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs12531711 0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs12537 0.827 0.280 22 30027471 3 prime UTR variant C/T snv 0.40 5
rs1270942 0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 11
rs12953 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs1308699981 0.807 0.440 1 161543085 missense variant G/A snv 4.0E-06 7
rs13101828 0.851 0.160 4 971932 intron variant A/G snv 0.43 6
rs13238352 0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 5
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs13389408 0.851 0.160 2 191068557 3 prime UTR variant T/C snv 7.4E-02 4
rs1341239 0.776 0.360 6 22303975 intron variant A/C snv 0.65 8
rs13447 0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1448674651 0.667 0.560 18 671384 missense variant G/A;C snv 4.0E-06 23