Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs7642134 3 86867732 intergenic variant A/G snv 0.55 1
rs7665931 4 103739525 intergenic variant C/T snv 9.7E-02 1
rs7821178 0.925 0.080 8 77181601 intergenic variant C/A;G;T snv 1
rs8014131 14 85497512 intron variant C/A snv 0.41 1
rs900145 11 13272358 upstream gene variant C/T snv 0.62 1
rs9555810 13 111529090 intergenic variant C/G;T snv 1
rs9635759 17 51536424 regulatory region variant G/A snv 0.25 1
rs320320
AKT3
1 243671884 intron variant A/G snv 0.30 1
rs6575793
BEGAIN
14 100565880 intron variant T/C snv 0.55 1
rs2479724
BYSL
6 41923244 intron variant T/C snv 0.62 1