rs587776422

Merged into

rs180177131

Orientation

minus

Stabilized

minus

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 38.1/142

Chromosome

16

Position

23621453

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776422
dbSNP (classic)	rs587776422
ClinGen	rs587776422
ebi	rs587776422
HLI	rs587776422
Exac	rs587776422
Gnomad	rs587776422
Varsome	rs587776422
LitVar	rs587776422
Map	rs587776422
PheGenI	rs587776422
Biobank	rs587776422
1000 genomes	rs587776422
hgdp	rs587776422
ensembl	rs587776422
geneview	rs587776422
scholar	rs587776422
google	rs587776422
pharmgkb	rs587776422
gwascentral	rs587776422
openSNP	rs587776422
23andMe	rs587776422
SNPshot	rs587776422
SNPdbe	rs587776422
MSV3d	rs587776422
GWAS Ctlg	rs587776422

Status

Merged into rs180177131

Max Magnitude

7

ClinVar
Risk
Alt
Reference	Rs587776422(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23632770delG
CLNSRC	PALB2 database
CLNACC	RCV000114586.2, RCV000133484.1, RCV000160811.1,