Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258 12 111280427 intron variant C/A;T snv 24
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs17030613 1 112648185 intron variant A/C snv 0.19 7
rs6015450 20 59176062 intron variant A/G snv 0.14 7
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs2131925 1 62560271 intron variant G/T snv 0.57 6
rs2643826 3 27521497 upstream gene variant C/T snv 0.56 6
rs35444 12 115114632 intergenic variant A/G snv 0.38 6
rs8068318 17 61406405 non coding transcript exon variant C/T snv 0.56 6
rs932764 10 94136183 intron variant A/G snv 0.38 6
rs10184428 2 164155317 intron variant C/A;G snv 5
rs1173766 5 32804422 intergenic variant T/C snv 0.57 5
rs12258967 10 18439030 intron variant C/G;T snv 5
rs167479 19 11416089 missense variant T/A;C;G snv 5
rs16849225 2 164050310 intron variant C/T snv 0.19 5
rs16896398 6 43294966 upstream gene variant A/T snv 0.42 5
rs1731249 2 26697157 intron variant T/A snv 0.48 5
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs3790604 1 112504257 intron variant C/A snv 7.8E-02 5
rs4373814 10 18131043 intergenic variant G/C;T snv 5
rs4980389 11 1871355 5 prime UTR variant G/A snv 0.35 5