Disease: Fasting blood glucose measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs10758593
GLIS3
0.827 0.240 9 4292083 intron variant G/A snv 0.45 4
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 4
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 4
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 4
rs10814916
GLIS3
0.851 0.200 9 4293150 intron variant A/C snv 0.57 3
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 3
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs1552224
ARAP1
1.000 0.080 11 72722053 5 prime UTR variant A/C snv 0.12 3
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs1783598
FCHSD2
1.000 0.080 11 73140418 intron variant C/G;T snv 3
rs2908289
GCK ; LOC105375257
1.000 0.080 7 44184343 intron variant G/A snv 0.20 3
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs4458523
WFS1
1.000 0.080 4 6288259 intron variant T/G snv 0.61 3