Rs17065323

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Orientationplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17065323(C;T)
Make rs17065323(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position44053652
is asnp
is mentioned by
dbSNPrs17065323
PheGenIrs17065323
nextbiors17065323
hapmaprs17065323
1000 genomesrs17065323
hgdprs17065323
ensemblrs17065323
gopubmedrs17065323
geneviewrs17065323
scholarrs17065323
googlers17065323
pharmgkbrs17065323
gwascentralrs17065323
openSNPrs17065323
23andMers17065323
23andMe allrs17065323
SNP Nexus

SNPshotrs17065323
SNPdbers17065323
MSV3drs17065323
GMAF0.06474
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs17065323
PubMedID [PMID 18759275OA-icon.png]
Condition Serum uric acid
Gene NR
Risk Allele
pValue 4.00E-006
OR 4.29
95% CI NR) mg/dl decrease in uric acid level



GET Evidence
rs17065323
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary