Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2328549
CDKAL1
6 20718009 intron variant A/T snv 0.18 1
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 3
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 3
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 3
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs6456368
CDKAL1
1.000 0.080 6 20659575 intron variant T/C snv 0.40 2
rs7767391
CDKAL1
1.000 0.080 6 20725009 intron variant T/C snv 0.28 2
rs9348440
CDKAL1
1.000 0.080 6 20641105 intron variant C/T snv 0.13 2
rs10229583 1.000 0.080 7 127606849 downstream gene variant G/A snv 0.23 1
rs1800574
HNF1A ; HNF1A-AS1
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 1
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 1
rs6935599
CDKAL1
1.000 0.080 6 20716864 intron variant A/G snv 0.31 1
rs7041847
GLIS3
1.000 0.080 9 4287466 intron variant A/G snv 0.37 1
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 1
rs7612463
UBE2E2
0.925 0.080 3 23294959 intron variant C/A;G snv 1
rs7747752
CDKAL1
1.000 0.080 6 20725192 intron variant G/C snv 0.34 1
rs9350276
CDKAL1
1.000 0.080 6 20740065 intron variant C/T snv 0.38 1
rs9505118
SSR1
1.000 0.080 6 7290204 intron variant A/G snv 0.37 1
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 3