Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs1084651 6 160668785 intron variant G/A snv 0.23 2
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 2
rs11246602 11 54607190 upstream gene variant A/G snv 0.11 2
rs11819350 10 17133943 upstream gene variant C/G;T snv 2
rs12720917 16 56985480 upstream gene variant T/C snv 0.10 2
rs1436424 16 56861122 upstream gene variant G/T snv 0.41 2
rs16969352 15 39577083 upstream gene variant T/C snv 5.1E-02 2
rs17158782 5 100726979 intergenic variant T/C snv 1.9E-02 2
rs2107369 16 68082115 intron variant T/G snv 0.18 2
rs2366858 7 80711306 regulatory region variant C/A snv 0.94 2
rs2652834 15 63104668 intron variant A/C;G;T snv 2
rs2814944 1.000 0.040 6 34585020 downstream gene variant G/A snv 0.20 2
rs34989676 5 148830704 downstream gene variant G/A snv 1.4E-02 2
rs386000 19 54288907 intergenic variant C/A;G snv 2
rs3922628 12 122724748 downstream gene variant T/A;C snv 2
rs4713865 6 35448531 intron variant C/G;T snv 2
rs4759361 12 122693733 intron variant T/A snv 0.21 2
rs4983559 14 104810872 downstream gene variant G/A;C snv 2
rs499974 11 75743976 downstream gene variant C/A snv 0.23 2
rs5953073 X 47634947 upstream gene variant A/G snv 0.12 2
rs6499861 16 56957583 upstream gene variant C/G snv 0.18 2
rs6499863 0.925 0.080 16 56958105 upstream gene variant G/A snv 0.19 2
rs6779158 3 10161878 upstream gene variant A/G snv 3.3E-02 2
rs7388248 8 143223183 regulatory region variant C/G snv 0.64 2