rs587776423

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/142

Chromosome

16

Position

23614003

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776423
dbSNP (classic)	rs587776423
ClinGen	rs587776423
ebi	rs587776423
HLI	rs587776423
Exac	rs587776423
Gnomad	rs587776423
Varsome	rs587776423
LitVar	rs587776423
Map	rs587776423
PheGenI	rs587776423
Biobank	rs587776423
1000 genomes	rs587776423
hgdp	rs587776423
ensembl	rs587776423
geneview	rs587776423
scholar	rs587776423
google	rs587776423
pharmgkb	rs587776423
gwascentral	rs587776423
openSNP	rs587776423
23andMe	rs587776423
SNPshot	rs587776423
SNPdbe	rs587776423
MSV3d	rs587776423
GWAS Ctlg	rs587776423

Max Magnitude

7

ClinVar
Risk	Rs587776423(C;C) rs587776423(T;T)
Alt	Rs587776423(C;C) rs587776423(T;T)
Reference	Rs587776423(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed	1
HGVS	NC_000016.9:g.23625324C>A; NC_000016.9:g.23625324C>G
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000130058.2, RCV000133485.1, RCV000164723.1, RCV000230297.1,