Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 4
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 4
rs1659127 16 14294448 intergenic variant G/A;C;T snv 2
rs4549631 6 126645162 intron variant T/C;G snv 2
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 2
rs7846385 8 77247943 intergenic variant T/C snv 0.23 2
rs1079866 0.925 0.080 7 41430495 intergenic variant C/G snv 0.13 1
rs10940138 5 67898641 intron variant C/T snv 0.21 1
rs13187289 5 134513486 upstream gene variant C/A;G snv 0.19 1
rs1364063 16 69554669 TF binding site variant T/C snv 0.35 1
rs1482582 4 103730396 intergenic variant A/C snv 0.34 1
rs1490384 6 126530014 intron variant C/G;T snv 1
rs17034020 4 103729516 intergenic variant G/A snv 9.8E-02 1
rs17034046 4 103738447 intergenic variant C/A;T snv 1
rs17196160 4 103736685 intergenic variant T/C snv 4.6E-02 1
rs17196407 4 103742364 intergenic variant C/T snv 4.1E-02 1
rs17249293 4 103735627 intergenic variant G/A;T snv 1
rs17249363 4 103736532 intergenic variant A/G snv 4.6E-02 1
rs2002675 3 185911780 downstream gene variant A/G snv 0.36 1
rs2947411 2 614168 intergenic variant A/G;T snv 1
rs4840086 6 99760562 intergenic variant A/G snv 0.33 1
rs6439371 3 132891908 intergenic variant G/A snv 0.63 1
rs6589964 11 122999975 intergenic variant A/C snv 0.54 1