rs152451

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;G)	0	Benign, according to ClinVar
(G;G)	0	Benign, according to ClinVar

Reference

GRCh38 38.1/142

Chromosome

16

Position

23634870

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs152451
dbSNP (classic)	rs152451
ClinGen	rs152451
ebi	rs152451
HLI	rs152451
Exac	rs152451
Gnomad	rs152451
Varsome	rs152451
LitVar	rs152451
Map	rs152451
PheGenI	rs152451
Biobank	rs152451
1000 genomes	rs152451
hgdp	rs152451
ensembl	rs152451
geneview	rs152451
scholar	rs152451
google	rs152451
pharmgkb	rs152451
gwascentral	rs152451
openSNP	rs152451
23andMe	rs152451
SNPshot	rs152451
SNPdbe	rs152451
MSV3d	rs152451
GWAS Ctlg	rs152451

Max Magnitude

0

[PMID 25636233] Association of PALB2 sequence variants with the risk of familial and early-onset breast cancer in a South-American population

ClinVar
Risk	Rs152451(G;G) rs152451(T;T)
Alt	Rs152451(G;G) rs152451(T;T)
Reference	Rs152451(A;A)
Significance	Other
Disease	Familial cancer of breast not specified Hereditary cancer-predisposing syndrome Fanconi anemia
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast not specified Hereditary cancer-predisposing syndrome Fanconi anemia
Reversed	1
HGVS	NC_000016.9:g.23646191T>C
CLNSRC	PALB2 database UniProtKB (protein)
CLNACC	RCV000114486.2, RCV000121747.3, RCV000128962.4, RCV000395533.1,