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rs4771450

From SNPedia

Orientationplus
Stabilizedplus
Make rs4771450(A;A)
Make rs4771450(A;G)
Make rs4771450(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position103317141
is asnp
is mentioned by
dbSNPrs4771450
ebirs4771450
HLIrs4771450
Exacrs4771450
Varsomers4771450
Maprs4771450
PheGenIrs4771450
hapmaprs4771450
1000 genomesrs4771450
hgdprs4771450
ensemblrs4771450
gopubmedrs4771450
geneviewrs4771450
scholarrs4771450
googlers4771450
pharmgkbrs4771450
gwascentralrs4771450
openSNPrs4771450
23andMers4771450
23andMe allrs4771450
SNP Nexus

SNPshotrs4771450
SNPdbers4771450
MSV3drs4771450
GWAS Ctlgrs4771450
GMAF0.3994
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs4771450
PubMedID [PMID 18759275OA-icon.png]
Condition Serum uric acid
Gene NR
Risk Allele
pValue 2.00E-006
OR 0.23
95% CI NR) mg/dl decrease in uric acid level



GET Evidence
rs4771450
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.619048
summary