Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs9366778
LINC02571 ; LOC112267902 ; HLA-B
0.925 0.120 6 31301396 intron variant G/A snv 0.47 6
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 3
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs1042725
HMGA2
0.882 0.080 12 65964567 3 prime UTR variant C/T snv 0.48 2
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 2
rs2421016
PLEKHA1
0.925 0.120 10 122407996 intron variant C/T snv 0.46 2
rs724577
LCORL
4 17991787 intron variant A/C snv 0.71 2
rs962554
ADGRG6
6 142413067 intron variant T/C snv 0.40 2
rs10788038 10 120117008 intergenic variant T/C snv 0.61 1
rs1151200
TENM4
11 79281641 intron variant T/C snv 0.50 1
rs11867479
KCNJ16
17 70094066 intron variant C/A;T snv 1
rs12340987 9 85156012 upstream gene variant A/G snv 0.19 1
rs13271368 8 125493898 intron variant C/T snv 0.18 1
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 1
rs1415701
L3MBTL3
6 130024690 intron variant G/A snv 0.31 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
rs2282978
LOC112268009 ; CDK6
7 92635096 intron variant T/C snv 0.38 1
rs2292626
PLEKHA1
0.925 0.120 10 122427198 intron variant C/T snv 0.46 1
rs2928148
INO80
15 41109352 intron variant G/A snv 0.44 1
rs2960051 18 30276169 intergenic variant C/T snv 0.84 1