Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10061469 5 73222321 intron variant T/C snv 0.37 1
rs10142466 14 68805067 intergenic variant A/C;G;T snv 1
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 1
rs10521318 16 85977731 intron variant C/G;T snv 1
rs11187157 10 92742487 TF binding site variant T/C snv 0.40 1
rs11641016 16 85981275 intron variant C/G snv 0.18 1
rs11677953 2 218256940 non coding transcript exon variant G/A snv 0.36 1
rs12585310 13 26954210 intergenic variant G/A snv 0.27 1
rs12627970 1.000 0.080 22 39325740 TF binding site variant A/G snv 0.19 1
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 1
rs1388585 12 40137889 downstream gene variant G/A snv 0.95 1
rs149169037 7 20537675 intergenic variant G/A snv 5.5E-02 1
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 1
rs1505992 5 40498475 intron variant A/T snv 0.61 1
rs17000400 4 75251521 regulatory region variant C/T snv 0.12 1
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 1
rs2472649 4 73991991 upstream gene variant A/G;T snv 1
rs2839073 21 45953845 regulatory region variant T/C snv 0.16 1
rs2847278 18 12778716 upstream gene variant C/T snv 0.83 1
rs3129891 0.851 0.160 6 32447303 downstream gene variant G/A snv 0.20 1
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 1
rs4552569 1.000 0.040 5 83877774 upstream gene variant C/T snv 0.75 1
rs4836519 5 130681594 intron variant T/A;C snv 1
rs4899554 14 75234518 downstream gene variant C/T snv 0.14 1
rs6935723 6 32713892 upstream gene variant T/C snv 0.29 1