rs587776406

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 38.1/142

Chromosome

16

Position

23637905

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776406
dbSNP (classic)	rs587776406
ClinGen	rs587776406
ebi	rs587776406
HLI	rs587776406
Exac	rs587776406
Gnomad	rs587776406
Varsome	rs587776406
LitVar	rs587776406
Map	rs587776406
PheGenI	rs587776406
Biobank	rs587776406
1000 genomes	rs587776406
hgdp	rs587776406
ensembl	rs587776406
geneview	rs587776406
scholar	rs587776406
google	rs587776406
pharmgkb	rs587776406
gwascentral	rs587776406
openSNP	rs587776406
23andMe	rs587776406
SNPshot	rs587776406
SNPdbe	rs587776406
MSV3d	rs587776406
GWAS Ctlg	rs587776406

Max Magnitude

7

ClinVar
Risk	Rs587776406(-;-)
Alt	Rs587776406(-;-)
Reference	Rs587776406(A;A)
Significance	Pathogenic
Disease	not provided Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	not provided Familial cancer of breast
Reversed	1
HGVS	NC_000016.9:g.23649226delT
CLNSRC	ClinVar
CLNACC	RCV000133474.1, RCV000461816.1,