rs587776413

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;G)	3	significantly increased risk of breast cancer
(G;G)	7	Fanconi anemia, complementation group N

Reference

GRCh38 38.1/142

Chromosome

16

Position

23634975

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776413
dbSNP (classic)	rs587776413
ClinGen	rs587776413
ebi	rs587776413
HLI	rs587776413
Exac	rs587776413
Gnomad	rs587776413
Varsome	rs587776413
LitVar	rs587776413
Map	rs587776413
PheGenI	rs587776413
Biobank	rs587776413
1000 genomes	rs587776413
hgdp	rs587776413
ensembl	rs587776413
geneview	rs587776413
scholar	rs587776413
google	rs587776413
pharmgkb	rs587776413
gwascentral	rs587776413
openSNP	rs587776413
23andMe	rs587776413
SNPshot	rs587776413
SNPdbe	rs587776413
MSV3d	rs587776413
GWAS Ctlg	rs587776413

Max Magnitude

7

ClinVar
Risk	Rs587776413(G;G)
Alt	Rs587776413(G;G)
Reference	Rs587776413(C;C)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23646296G>C
CLNSRC	ClinVar
CLNACC	RCV000133475.1, RCV000454158.1,