rs447529

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	Benign variant
(C;G)	0	benign variant
(G;G)	0	common in clinvar

Reference

GRCh38 38.1/141

Chromosome

16

Position

23622102

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs447529
dbSNP (classic)	rs447529
ClinGen	rs447529
ebi	rs447529
HLI	rs447529
Exac	rs447529
Gnomad	rs447529
Varsome	rs447529
LitVar	rs447529
Map	rs447529
PheGenI	rs447529
Biobank	rs447529
1000 genomes	rs447529
hgdp	rs447529
ensembl	rs447529
geneview	rs447529
scholar	rs447529
google	rs447529
pharmgkb	rs447529
gwascentral	rs447529
openSNP	rs447529
23andMe	rs447529
SNPshot	rs447529
SNPdbe	rs447529
MSV3d	rs447529
GWAS Ctlg	rs447529

GMAF

0.1455

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 19921424] Five common single nucleotide polymorphisms in the PALB2 gene and susceptibility to breast cancer in eastern Chinese population

ClinVar
Risk	Rs447529(C;C)
Alt	Rs447529(C;C)
Reference	Rs447529(G;G)
Significance	Non-pathogenic
Disease	Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000016.9:g.23633423C>G
CLNSRC	PALB2 database
CLNACC	RCV000114584.1,

[PMID 26981788] Role of PALB2 Polymorphisms with Regard to Susceptibility to Female Breast Cancer Risk in the Chinese Population.