Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11677452 2 102248776 downstream gene variant A/G;T snv 1
rs11687768 2 102409278 upstream gene variant A/G;T snv 1
rs11690644 2 102297754 regulatory region variant A/G snv 9.9E-02 1
rs11693955 2 102412705 downstream gene variant A/T snv 0.23 1
rs11776367 8 80347816 intron variant A/T snv 0.50 1
rs12203586 6 32711814 upstream gene variant G/A;C snv 1
rs12233670 4 38785595 upstream gene variant C/T snv 0.32 1
rs12261421 10 8916848 downstream gene variant C/T snv 5.1E-02 1
rs12413578 0.882 0.160 10 9007290 intergenic variant C/G;T snv 1
rs12472359 2 197723141 intron variant T/A;C snv 1
rs12528368 6 32685866 TF binding site variant T/C snv 0.14 1
rs12529093 6 32448081 downstream gene variant A/G snv 0.13 1
rs12543811 1.000 0.080 8 80366650 intron variant G/A snv 0.62 1
rs12622674 2 197687088 intergenic variant G/A snv 0.52 1
rs12659961 5 110851305 intergenic variant T/C snv 0.30 1
rs12712148 2 102409087 upstream gene variant G/A snv 0.22 1
rs12789493 11 76564659 regulatory region variant T/C snv 0.56 1
rs12991737 2 102401668 downstream gene variant T/A snv 0.22 1
rs13027294 2 102243614 downstream gene variant G/C;T snv 1
rs13209234 6 32448198 downstream gene variant G/A snv 0.13 1
rs13270496 8 80368431 intron variant A/C snv 0.49 1
rs13275219 8 80347591 intron variant T/C snv 0.61 1
rs13275449 8 80363878 intron variant G/A snv 0.62 1
rs13437092 6 31387279 upstream gene variant G/T snv 0.32 1
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 1