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rs6085920

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs6085920(A;T)
Make rs6085920(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position7199409
GeneLOC101929265
is asnp
is mentioned by
dbSNPrs6085920
ebirs6085920
HLIrs6085920
Exacrs6085920
Varsomers6085920
Maprs6085920
PheGenIrs6085920
hapmaprs6085920
1000 genomesrs6085920
hgdprs6085920
ensemblrs6085920
gopubmedrs6085920
geneviewrs6085920
scholarrs6085920
googlers6085920
pharmgkbrs6085920
gwascentralrs6085920
openSNPrs6085920
23andMers6085920
23andMe allrs6085920
SNP Nexus

SNPshotrs6085920
SNPdbers6085920
MSV3drs6085920
GWAS Ctlgrs6085920
GMAF0.2181
Max Magnitude0
? (A;A) (A;T) (T;T) 28
GWAS
SNP rs6085920
PubMedID [PMID 18759275OA-icon.png]
Condition Serum uric acid
Gene NR
Risk Allele
pValue 6.00E-006
OR 0.4
95% CI NR) mg/dl decrease in uric acid level



GET Evidence
rs6085920
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.71875
summary