rs180177126

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/141

Chromosome

16

Position

23623044

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs180177126
dbSNP (classic)	rs180177126
ClinGen	rs180177126
ebi	rs180177126
HLI	rs180177126
Exac	rs180177126
Gnomad	rs180177126
Varsome	rs180177126
LitVar	rs180177126
Map	rs180177126
PheGenI	rs180177126
Biobank	rs180177126
1000 genomes	rs180177126
hgdp	rs180177126
ensembl	rs180177126
geneview	rs180177126
scholar	rs180177126
google	rs180177126
pharmgkb	rs180177126
gwascentral	rs180177126
openSNP	rs180177126
23andMe	rs180177126
SNPshot	rs180177126
SNPdbe	rs180177126
MSV3d	rs180177126
GWAS Ctlg	rs180177126

Merged from

Rs587776421

Max Magnitude

7

ClinVar
Risk	Rs180177126(-;-)
Alt	Rs180177126(-;-)
Reference	Rs180177126(AA;AA)
Significance	Pathogenic
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	1
HGVS	NC_000016.9:g.23634365_23634366delTT
CLNSRC	PALB2 database
CLNACC	RCV000114575.4, RCV000132234.6, RCV000133483.2,

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