rs16940342

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	0	Considered benign according to ClinVar
(G;G)	0	Considered benign according to ClinVar

Reference

GRCh38 38.1/141

Chromosome

16

Position

23633265

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs16940342
dbSNP (classic)	rs16940342
ClinGen	rs16940342
ebi	rs16940342
HLI	rs16940342
Exac	rs16940342
Gnomad	rs16940342
Varsome	rs16940342
LitVar	rs16940342
Map	rs16940342
PheGenI	rs16940342
Biobank	rs16940342
1000 genomes	rs16940342
hgdp	rs16940342
ensembl	rs16940342
geneview	rs16940342
scholar	rs16940342
google	rs16940342
pharmgkb	rs16940342
gwascentral	rs16940342
openSNP	rs16940342
23andMe	rs16940342
SNPshot	rs16940342
SNPdbe	rs16940342
MSV3d	rs16940342
GWAS Ctlg	rs16940342

GMAF

0.1873

Max Magnitude

0

?	(A;A) (A;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	rs16940342(C;C) Rs16940342(G;G) rs16940342(T;T)
Alt	rs16940342(C;C) Rs16940342(G;G) rs16940342(T;T)
Reference	Rs16940342(A;A)
Significance	Non-pathogenic
Disease	Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000016.9:g.23644586A>G
CLNSRC	PALB2 database
CLNACC	RCV000114488.1,

[PMID 18794107] Association of common PALB2 polymorphisms with breast cancer risk: a case-control study.

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