rs180177127

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(;)	0	common in clinvar
(-;-)	0	common/normal
(-;T)	3	increased risk for breast cancer
(T;T)	7	Fanconi anemia, complementation group N

Reference

GRCh38 38.1/141

Chromosome

16

Position

23622982

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs180177127
dbSNP (classic)	rs180177127
ClinGen	rs180177127
ebi	rs180177127
HLI	rs180177127
Exac	rs180177127
Gnomad	rs180177127
Varsome	rs180177127
LitVar	rs180177127
Map	rs180177127
PheGenI	rs180177127
Biobank	rs180177127
1000 genomes	rs180177127
hgdp	rs180177127
ensembl	rs180177127
geneview	rs180177127
scholar	rs180177127
google	rs180177127
pharmgkb	rs180177127
gwascentral	rs180177127
openSNP	rs180177127
23andMe	rs180177127
SNPshot	rs180177127
SNPdbe	rs180177127
MSV3d	rs180177127
GWAS Ctlg	rs180177127

Max Magnitude

7

ClinVar
Risk	Rs180177127(T;T)
Alt	Rs180177127(T;T)
Reference	Rs180177127(-;-)
Significance	Other
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23634304dupA
CLNSRC	PALB2 database
CLNACC	RCV000114576.4, RCV000213482.2,

[PMID 17200668] PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.