Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 2
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs503279
FUT2 ; LOC105447645
19 48705753 3 prime UTR variant T/C snv 0.48 2
rs6499165
SLC7A6OS ; SLC7A6
16 68292297 non coding transcript exon variant A/C snv 0.80 2
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs9332998
CYP4A11
1 46938514 intron variant T/C snv 0.16 2
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 4