Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 6
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 5
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 3
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 3
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 2
rs12807809 0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20 2
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs17645023 1.000 0.040 17 66920916 intergenic variant A/T snv 0.22 2
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 2
rs424232 0.882 0.240 6 32240547 intergenic variant C/A;T snv 2
rs4949526 1.000 0.040 1 29959372 intergenic variant T/C snv 0.54 2
rs6589386 1.000 0.040 11 113573031 intergenic variant C/T snv 0.36 2
rs6913660 1.000 0.040 6 27123646 upstream gene variant C/A snv 0.14 2
rs6932590 1.000 0.040 6 27281152 downstream gene variant T/C snv 0.26 2
rs7776351 0.925 0.080 6 27758952 upstream gene variant C/T snv 0.34 2
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 2
rs1001684 1.000 0.040 5 40810324 intergenic variant C/A snv 0.29 1
rs10135277 1.000 0.040 14 35354025 TF binding site variant C/T snv 0.43 1
rs10429924 1.000 0.040 1 244227262 intergenic variant C/T snv 8.8E-02 1
rs10498146 1.000 0.040 2 222987318 intergenic variant A/G snv 6.2E-02 1
rs10789369 1.000 0.040 1 73359226 downstream gene variant A/G;T snv 1