Disease: elevated blood glucose level
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
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs2657879
GLS2 ; SPRYD4
1.000 0.080 12 56471554 missense variant A/G snv 0.17 0.15 5
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 4
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 4
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 3