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rs2073376

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs2073376(A;G)
Make rs2073376(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position46431839
GenePCNT
is asnp
is mentioned by
dbSNPrs2073376
ebirs2073376
HLIrs2073376
Exacrs2073376
Varsomers2073376
Maprs2073376
PheGenIrs2073376
hapmaprs2073376
1000 genomesrs2073376
hgdprs2073376
ensemblrs2073376
gopubmedrs2073376
geneviewrs2073376
scholarrs2073376
googlers2073376
pharmgkbrs2073376
gwascentralrs2073376
openSNPrs2073376
23andMers2073376
23andMe allrs2073376
SNP Nexus

SNPshotrs2073376
SNPdbers2073376
MSV3drs2073376
GWAS Ctlgrs2073376
GMAF0.3237
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 19448849OA-icon.png] Positive association of the pericentrin (PCNT) gene with major depressive disorder in the Japanese population


GET Evidence
PCNT-Q2792R
aa_change Gln2792Arg
aa_change_short Q2792R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.693437
summary



ClinVar
Risk rs2073376(G;G)
Alt rs2073376(G;G)
Reference rs2073376(A;A)
Significance Non-pathogenic
Disease not specified
Variation info
Gene PCNT
CLNDBN not specified
Reversed 0
HGVS NC_000021.8:g.47851753A>G
CLNSRC ClinVar University of Chicago
CLNACC RCV000147222.4,