rs587781840

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23623001

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587781840
dbSNP (classic)	rs587781840
ClinGen	rs587781840
ebi	rs587781840
HLI	rs587781840
Exac	rs587781840
Gnomad	rs587781840
Varsome	rs587781840
LitVar	rs587781840
Map	rs587781840
PheGenI	rs587781840
Biobank	rs587781840
1000 genomes	rs587781840
hgdp	rs587781840
ensembl	rs587781840
geneview	rs587781840
scholar	rs587781840
google	rs587781840
pharmgkb	rs587781840
gwascentral	rs587781840
openSNP	rs587781840
23andMe	rs587781840
SNPshot	rs587781840
SNPdbe	rs587781840
MSV3d	rs587781840
GWAS Ctlg	rs587781840

Max Magnitude

7

ClinVar
Risk	Rs587781840(-;-)
Alt	Rs587781840(-;-)
Reference	Rs587781840(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed	1
HGVS	NC_000016.9:g.23634322delT
CLNSRC
CLNACC	RCV000130137.4, RCV000476828.1, RCV000481028.1,