Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10788038 10 120117008 intergenic variant T/C snv 0.61 1
rs12340987 9 85156012 upstream gene variant A/G snv 0.19 1
rs13271368 8 125493898 intron variant C/T snv 0.18 1
rs17064002 13 42996665 upstream gene variant C/T snv 1.8E-02 1
rs17138114 6 4379277 intron variant A/G snv 0.10 1
rs2960051 18 30276169 intergenic variant C/T snv 0.84 1
rs4432842 1.000 0.080 5 57876251 intergenic variant T/C snv 0.45 1
rs4564656 18 30301067 intron variant G/A snv 0.76 1
rs6508654 18 30302598 intron variant T/C snv 0.81 1
rs7742369 6 34197944 TF binding site variant A/G snv 0.30 1
rs7968682 12 65978100 intergenic variant G/T snv 0.56 1
rs930811 9 2696555 intergenic variant G/A snv 0.47 1
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs9883204
ADCY5
3 123377973 intron variant T/A;C snv 1
rs962554
ADGRG6
6 142413067 intron variant T/C snv 0.40 2
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 1
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 2
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs798489
GNA12 ; AMZ1
7 2762169 splice donor variant C/T snv 0.20 1
rs7780752
GNGT1
7 93612328 intron variant T/C snv 0.27 1
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 2
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 1
rs8756
HMGA2
0.882 0.200 12 65965972 3 prime UTR variant C/A snv 0.56 1