Disease: Fasting blood glucose measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs174576
FADS2
0.851 0.200 11 61836038 intron variant C/A;T snv 9
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
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 5
rs174583
FADS2
0.807 0.320 11 61842278 intron variant C/T snv 0.35 5
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 4
rs853789
ABCB11
2 168944978 intron variant A/G;T snv 0.75 3
rs563694
ABCB11
2 168917561 intron variant C/A snv 0.75 2
rs853787
ABCB11
2 168945742 intron variant G/A;T snv 2