Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs4458523
WFS1
1.000 0.080 4 6288259 intron variant T/G snv 0.61 3
rs16913693
ELP1
9 108918079 intron variant T/G snv 8.4E-02 2
rs2300615
GLP1R
6 39071727 intron variant T/G snv 0.17 2
rs3138708
SLC2A2
3 171009914 intron variant T/G snv 3.1E-02 2
rs983309 8 9320222 intron variant T/G snv 0.82 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs3816725
MADD
11 47284118 intron variant T/C;G snv 2
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 7
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 6
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 3
rs4245555
GRB10
1.000 0.120 7 50593712 intron variant T/C snv 0.32 3
rs4502156 1.000 0.080 15 62090956 intergenic variant T/C snv 0.55 3
rs11039182
MADD
11 47325172 intron variant T/C snv 0.19 2
rs12440695 15 62142957 regulatory region variant T/C snv 0.32 2
rs1280 3 170995501 intron variant T/C snv 0.20 2
rs1401419
CRY2
1.000 0.040 11 45858188 intron variant T/C snv 0.39 2
rs17265513
ZHX3
0.925 0.160 20 41203988 missense variant T/C snv 0.14 0.14 2
rs2268575
GCK ; LOC105375258
7 44149675 intron variant T/C snv 0.18 2