Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4118325 1 107035210 intergenic variant G/A;T snv 1
rs6925255 6 79756407 regulatory region variant A/C;G;T snv 1
rs294588 5 163571509 regulatory region variant T/C snv 0.70 1
rs11128951 3 20334054 intron variant A/G snv 0.19 1
rs4518581 7 118970601 intergenic variant G/A snv 0.86 1
rs6466686 7 118996763 intergenic variant C/T snv 0.58 1
rs6785365 3 133543601 upstream gene variant A/G snv 0.65 1
rs10281955 7 118944637 intergenic variant G/A snv 0.86 1
rs4268066 7 118961051 intergenic variant C/T snv 0.86 1
rs17144687 5 118824240 intergenic variant A/C snv 4.5E-02 1
rs6763627 3 133543723 upstream gene variant C/G;T snv 1
rs10935068 3 133543963 upstream gene variant T/A;G snv 1
rs10433415 3 133566686 intergenic variant G/T snv 0.57 1
rs4017074 3 133541583 downstream gene variant T/C snv 0.71 1
rs10953881 7 118968071 intergenic variant C/G;T snv 1
rs4854723 3 133535414 regulatory region variant A/C snv 0.52 1
rs7812233 7 118978108 intergenic variant G/A snv 0.86 1
rs10953885 7 118968349 intergenic variant T/A;C snv 1
rs4730908 7 119017956 intergenic variant C/G;T snv 1
rs3860498 3 133541672 downstream gene variant T/A;C snv 1
rs4854727 3 133539041 downstream gene variant A/G snv 0.65 1
rs4854733 3 133568221 intergenic variant A/G;T snv 1
rs170099 7 119360158 intergenic variant C/T snv 0.84 1
rs2749097 1 63661797 downstream gene variant C/G snv 0.19 1
rs7614812 3 133545407 upstream gene variant C/A snv 0.62 1