rs515726065

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	7	Fanconi anemia, complementation group N
(-;T)	5	PALB2-related cancer risk
(T;T)	0	common in clinvar

Reference

GRCh38 38.1/141

Chromosome

16

Position

23635232

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs515726065
dbSNP (classic)	rs515726065
ClinGen	rs515726065
ebi	rs515726065
HLI	rs515726065
Exac	rs515726065
Gnomad	rs515726065
Varsome	rs515726065
LitVar	rs515726065
Map	rs515726065
PheGenI	rs515726065
Biobank	rs515726065
1000 genomes	rs515726065
hgdp	rs515726065
ensembl	rs515726065
geneview	rs515726065
scholar	rs515726065
google	rs515726065
pharmgkb	rs515726065
gwascentral	rs515726065
openSNP	rs515726065
23andMe	rs515726065
SNPshot	rs515726065
SNPdbe	rs515726065
MSV3d	rs515726065
GWAS Ctlg	rs515726065

Max Magnitude

7

[PMID 25099575] Breast-Cancer Risk in Families with Mutations in PALB2

see also ClinVar (where clinical significance = pathogenic)

ClinVar
Risk	Rs515726065(-;-)
Alt	Rs515726065(-;-)
Reference	Rs515726065(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Pancreatic cancer 3
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast Pancreatic cancer 3
Reversed	0
HGVS	NC_000016.9:g.23646553delT
CLNSRC	PALB2 database
CLNACC	RCV000114467.1, RCV000114468.1,