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rs493573

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs493573(C;T)
Make rs493573(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position64789582
GeneMAP4K2
is asnp
is mentioned by
dbSNPrs493573
ebirs493573
HLIrs493573
Exacrs493573
Varsomers493573
Maprs493573
PheGenIrs493573
hapmaprs493573
1000 genomesrs493573
hgdprs493573
ensemblrs493573
gopubmedrs493573
geneviewrs493573
scholarrs493573
googlers493573
pharmgkbrs493573
gwascentralrs493573
openSNPrs493573
23andMers493573
23andMe allrs493573
SNP Nexus

SNPshotrs493573
SNPdbers493573
MSV3drs493573
GWAS Ctlgrs493573
GMAF0.004591
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21768215OA-icon.png]
Trait
Title Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele.
Risk Allele A
P-val 2E-17
Odds Ratio 0.8000 [NR] mg/dl decrease