Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs6499165
SLC7A6OS ; SLC7A6
16 68292297 non coding transcript exon variant A/C snv 0.80 2
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 6
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 7
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 2
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
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
rs272889
SLC22A4 ; MIR3936HG
5 132329685 intron variant A/G snv 0.64 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 2
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs1447352 11 92989595 downstream gene variant G/A snv 0.55 2
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 1
rs10885409
TCF7L2
1.000 0.080 10 113048313 intron variant T/C snv 0.54 1
rs503279
FUT2 ; LOC105447645
19 48705753 3 prime UTR variant T/C snv 0.48 2
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs12670403
LOC101927609 ; AHR
7 17269655 intron variant C/A snv 0.46 2
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 1
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10