rs2073380

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs2073380(A;C)

Make rs2073380(C;C)

Reference

GRCh38 38.1/141

Chromosome

21

Position

46443844

Gene

PCNT

is a	snp
is	mentioned by
dbSNP	rs2073380
dbSNP (classic)	rs2073380
ClinGen	rs2073380
ebi	rs2073380
HLI	rs2073380
Exac	rs2073380
Gnomad	rs2073380
Varsome	rs2073380
LitVar	rs2073380
Map	rs2073380
PheGenI	rs2073380
Biobank	rs2073380
1000 genomes	rs2073380
hgdp	rs2073380
ensembl	rs2073380
geneview	rs2073380
scholar	rs2073380
google	rs2073380
pharmgkb	rs2073380
gwascentral	rs2073380
openSNP	rs2073380
23andMe	rs2073380
SNPshot	rs2073380
SNPdbe	rs2073380
MSV3d	rs2073380
GWAS Ctlg	rs2073380

GMAF

0.2346

Max Magnitude

0

?

(A;A) (A;C) (C;C)

28

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

[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

ClinVar
Risk	rs2073380(C;C)
Alt	rs2073380(C;C)
Reference	Rs2073380(A;A)
Significance	Non-pathogenic
Disease	not specified Microcephalic Osteodysplastic Primordial Dwarfism
Variation	info
Gene	PCNT
CLNDBN	not specified Microcephalic Osteodysplastic Primordial Dwarfism
Reversed	0
HGVS	NC_000021.8:g.47863757A>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000147250.1, RCV000348673.1,