Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10761587 0.925 0.120 10 50889433 upstream gene variant T/C snv 0.69 2
rs10792438 0.925 0.120 11 64535054 downstream gene variant G/A snv 0.28 2
rs10896032 0.925 0.120 11 65691948 upstream gene variant C/A snv 0.34 2
rs10938761 0.925 0.120 4 10341099 intergenic variant C/T snv 0.89 2
rs10939427 0.925 0.120 4 9626914 intron variant G/A;C;T snv 2
rs10939436 0.925 0.120 4 9645511 intron variant T/A;C;G snv 2
rs10939472 0.925 0.120 4 9719992 intergenic variant G/A;C snv 2
rs10939504 0.925 0.120 4 9765746 regulatory region variant A/G snv 0.94 2
rs10957767 0.925 0.120 8 75579950 intergenic variant A/G snv 0.66 2
rs1114568 0.925 0.120 4 88238667 intergenic variant G/A snv 0.50 2
rs11231808 0.925 0.120 11 64534869 downstream gene variant G/A snv 0.34 2
rs11231816 0.925 0.120 11 64544931 intergenic variant G/A snv 0.32 2
rs11675428 0.925 0.120 2 27419867 intergenic variant A/C snv 0.11 2
rs11721485 0.925 0.120 4 10410930 upstream gene variant T/C snv 7.0E-02 2
rs11722202 0.925 0.120 4 9442168 upstream gene variant C/G;T snv 2
rs11722359 0.925 0.120 4 9506565 intergenic variant A/C;G snv 2
rs11722643 0.925 0.120 4 10125860 intergenic variant C/G;T snv 2
rs11724183 0.925 0.120 4 9608270 intron variant A/G snv 4.6E-02 2
rs11724536 0.925 0.120 4 10388665 regulatory region variant T/C snv 0.89 2
rs11724606 0.925 0.120 4 9718820 regulatory region variant G/A snv 0.11 2
rs11727261 0.925 0.120 4 10361858 intergenic variant A/G snv 0.89 2
rs11727674 0.925 0.120 4 9718357 intergenic variant C/T snv 0.34 2
rs11727873 0.925 0.120 4 9756845 downstream gene variant T/C;G snv 2
rs11729600 0.925 0.120 4 9763062 regulatory region variant T/C snv 0.94 2
rs11729997 0.925 0.120 4 88249907 intergenic variant C/A;G snv 0.42 2