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rs2249057

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2249057(A;A)
Make rs2249057(A;C)
ReferenceGRCh38 38.1/141
Chromosome21
Position46353189
GenePCNT
is asnp
is mentioned by
dbSNPrs2249057
ebirs2249057
HLIrs2249057
Exacrs2249057
Varsomers2249057
Maprs2249057
PheGenIrs2249057
hapmaprs2249057
1000 genomesrs2249057
hgdprs2249057
ensemblrs2249057
gopubmedrs2249057
geneviewrs2249057
scholarrs2249057
googlers2249057
pharmgkbrs2249057
gwascentralrs2249057
openSNPrs2249057
23andMers2249057
23andMe allrs2249057
SNP Nexus

SNPshotrs2249057
SNPdbers2249057
MSV3drs2249057
GWAS Ctlgrs2249057
GMAF0.3099
Max Magnitude0
? (A;A) (A;C) (C;C) 28

[PMID 19191256] Association studies and gene expression analyses of the DISC1-interacting molecules, pericentrin 2 (PCNT2) and DISC1-binding zinc finger protein (DBZ), with schizophrenia and with bipolar disorder


[PMID 19448849OA-icon.png] Positive association of the pericentrin (PCNT) gene with major depressive disorder in the Japanese population.


[PMID 20403199OA-icon.png] High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta.


ClinVar
Risk rs2249057(A;A)
Alt rs2249057(A;A)
Reference rs2249057(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene PCNT
CLNDBN not specified
Reversed 0
HGVS NC_000021.8:g.47773103C>A
CLNSRC ClinVar University of Chicago
CLNACC RCV000147090.1,