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
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 6
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 6
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs11603334
ARAP1
1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 4
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 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
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs11605924
CRY2
1.000 0.080 11 45851540 intron variant A/C snv 0.39 3
rs11920090
SLC2A2
1.000 0.040 3 170999732 intron variant T/A snv 0.20 3
rs1371614
DPYSL5
2 26930006 intron variant C/T snv 0.29 3
rs1483121 1.000 0.080 11 48311808 downstream gene variant G/A snv 9.7E-02 3
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 3
rs7944584
MADD
1.000 0.080 11 47314769 intron variant A/T snv 0.19 3