rs753153576

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	3	2-4 fold higher risk for breast cancer, depending on family history
(T;T)	7	Fanconi anemia, complementation group N

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23626235

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs753153576
dbSNP (classic)	rs753153576
ClinGen	rs753153576
ebi	rs753153576
HLI	rs753153576
Exac	rs753153576
Gnomad	rs753153576
Varsome	rs753153576
LitVar	rs753153576
Map	rs753153576
PheGenI	rs753153576
Biobank	rs753153576
1000 genomes	rs753153576
hgdp	rs753153576
ensembl	rs753153576
geneview	rs753153576
scholar	rs753153576
google	rs753153576
pharmgkb	rs753153576
gwascentral	rs753153576
openSNP	rs753153576
23andMe	rs753153576
SNPshot	rs753153576
SNPdbe	rs753153576
MSV3d	rs753153576
GWAS Ctlg	rs753153576

Merged from

Rs786202646

Max Magnitude

7

ClinVar
Risk	rs753153576(A;A) rs753153576(G;G) Rs753153576(T;T)
Alt	rs753153576(A;A) rs753153576(G;G) Rs753153576(T;T)
Reference	Rs753153576(C;C)
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	0
HGVS	NC_000016.9:g.23637556C>A; NC_000016.9:g.23637556C>G
CLNSRC
CLNACC	RCV000165555.3, RCV000487378.1, RCV000409294.1,