rs180177131

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/141

Chromosome

16

Position

23621449

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs180177131
dbSNP (classic)	rs180177131
ClinGen	rs180177131
ebi	rs180177131
HLI	rs180177131
Exac	rs180177131
Gnomad	rs180177131
Varsome	rs180177131
LitVar	rs180177131
Map	rs180177131
PheGenI	rs180177131
Biobank	rs180177131
1000 genomes	rs180177131
hgdp	rs180177131
ensembl	rs180177131
geneview	rs180177131
scholar	rs180177131
google	rs180177131
pharmgkb	rs180177131
gwascentral	rs180177131
openSNP	rs180177131
23andMe	rs180177131
SNPshot	rs180177131
SNPdbe	rs180177131
MSV3d	rs180177131
GWAS Ctlg	rs180177131

Merged from

Rs587776422

Max Magnitude

7

ClinVar
Risk	Rs180177131(-;-)
Alt	Rs180177131(-;-)
Reference	Rs180177131(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast not provided
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast not provided
Reversed	1
HGVS	NC_000016.9:g.23632770delG
CLNSRC	PALB2 database
CLNACC	RCV000114586.2, RCV000133484.2,

[PMID 21285249] Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer.