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rs4668338

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4668338(C;G)
Make rs4668338(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position170876715
is asnp
is mentioned by
dbSNPrs4668338
ebirs4668338
HLIrs4668338
Exacrs4668338
Varsomers4668338
Maprs4668338
PheGenIrs4668338
hapmaprs4668338
1000 genomesrs4668338
hgdprs4668338
ensemblrs4668338
gopubmedrs4668338
geneviewrs4668338
scholarrs4668338
googlers4668338
pharmgkbrs4668338
gwascentralrs4668338
openSNPrs4668338
23andMers4668338
23andMe allrs4668338
SNP Nexus

SNPshotrs4668338
SNPdbers4668338
MSV3drs4668338
GWAS Ctlgrs4668338
GMAF0.1414
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS
SNP rs4668338
PubMedID [PMID 18759275OA-icon.png]
Condition Serum uric acid
Gene NR
Risk Allele
pValue 3.00E-006
OR 4.29
95% CI NR) mg/dl decrease in uric acid level



GET Evidence
rs4668338
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.859375
summary