Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 1
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 1
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 1
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 1
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 1
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 2
rs1447352 11 92989595 downstream gene variant G/A snv 0.55 2
rs1495743 8 18415790 intergenic variant G/A;C snv 2
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 2
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs2518049
AKR1C3
10 5095844 intron variant A/G;T snv 2
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs9332998
CYP4A11
1 46938514 intron variant T/C snv 0.16 2
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
rs503279
FUT2 ; LOC105447645
19 48705753 3 prime UTR variant T/C snv 0.48 2
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2