Disease: Uric acid measurement (procedure)
Source: GWASCAT ×
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 55
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 3
rs703978
ZMIZ1
1.000 0.080 10 79184390 intron variant C/G;T snv 0.68 3
rs1800574
HNF1A ; HNF1A-AS1
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 2
rs35612982
CDKAL1
1.000 0.080 6 20682391 intron variant T/C snv 0.29 2