rs515726117

Orientation

plus

Stabilized

plus

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

Reference

GRCh38 38.1/141

Chromosome

16

Position

23603658

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs515726117
dbSNP (classic)	rs515726117
ClinGen	rs515726117
ebi	rs515726117
HLI	rs515726117
Exac	rs515726117
Gnomad	rs515726117
Varsome	rs515726117
LitVar	rs515726117
Map	rs515726117
PheGenI	rs515726117
Biobank	rs515726117
1000 genomes	rs515726117
hgdp	rs515726117
ensembl	rs515726117
geneview	rs515726117
scholar	rs515726117
google	rs515726117
pharmgkb	rs515726117
gwascentral	rs515726117
openSNP	rs515726117
23andMe	rs515726117
SNPshot	rs515726117
SNPdbe	rs515726117
MSV3d	rs515726117
GWAS Ctlg	rs515726117

Max Magnitude

7

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

ClinVar
Risk	Rs515726117(-;-)
Alt	Rs515726117(-;-)
Reference	Rs515726117(C;C)
Significance	Other
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000016.9:g.23614979delC
CLNSRC	PALB2 database
CLNACC	RCV000114624.7, RCV000130740.3, RCV000235614.2,