rs180177138

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/141

Chromosome

16

Position

23603523

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs180177138
dbSNP (classic)	rs180177138
ClinGen	rs180177138
ebi	rs180177138
HLI	rs180177138
Exac	rs180177138
Gnomad	rs180177138
Varsome	rs180177138
LitVar	rs180177138
Map	rs180177138
PheGenI	rs180177138
Biobank	rs180177138
1000 genomes	rs180177138
hgdp	rs180177138
ensembl	rs180177138
geneview	rs180177138
scholar	rs180177138
google	rs180177138
pharmgkb	rs180177138
gwascentral	rs180177138
openSNP	rs180177138
23andMe	rs180177138
SNPshot	rs180177138
SNPdbe	rs180177138
MSV3d	rs180177138
GWAS Ctlg	rs180177138

Max Magnitude

7

ClinVar
Risk	Rs180177138(-;-)
Alt	Rs180177138(-;-)
Reference	Rs180177138(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Pancreatic cancer 3
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast Pancreatic cancer 3
Reversed	1
HGVS	NC_000016.9:g.23614844delC
CLNSRC	PALB2 database
CLNACC	RCV000114631.1, RCV000114632.1,

[PMID 21184274] PALB2 germline mutations in familial breast cancer cases with personal and family history of pancreatic cancer.