Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4715210 6 50929538 regulatory region variant C/G;T snv 2
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs4854349 2 647861 intergenic variant T/C snv 0.77 2
rs516636 1 177886382 intron variant C/A snv 0.17 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs571312 1.000 0.080 18 60172536 intergenic variant C/A snv 0.26 2
rs574367 1 177904075 intron variant G/T snv 0.16 2
rs591166 18 60174356 intergenic variant T/A snv 0.52 2
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 2
rs713586 0.925 0.160 2 24935139 intergenic variant T/C snv 0.58 2
rs7173964 1.000 0.080 15 62104743 regulatory region variant G/A snv 0.49 2
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 2
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 2
rs867559 9 126703046 non coding transcript exon variant A/G snv 0.26 2
rs939583 1.000 0.080 2 622531 intergenic variant C/T snv 0.85 2
rs9473924 6 50866444 intergenic variant G/T snv 0.33 2
rs10182181 1.000 0.080 2 24927427 intergenic variant A/G snv 0.57 1
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 1
rs11041816 11 8222251 downstream gene variant A/G snv 0.36 1
rs11127485 1.000 0.080 2 632028 intergenic variant C/T snv 0.85 1
rs12198798 6 12509895 upstream gene variant T/C snv 0.17 1
rs12422552 0.925 0.080 12 14260997 regulatory region variant G/C snv 0.30 1
rs12955983 1.000 0.080 18 60205756 intergenic variant A/G snv 0.20 1
rs1564981 16 50952397 intergenic variant G/A snv 0.60 1