rs587776425

Orientation

minus

Stabilized

minus

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

Reference

GRCh38 38.1/142

Chromosome

16

Position

23603593

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587776425
dbSNP (classic)	rs587776425
ClinGen	rs587776425
ebi	rs587776425
HLI	rs587776425
Exac	rs587776425
Gnomad	rs587776425
Varsome	rs587776425
LitVar	rs587776425
Map	rs587776425
PheGenI	rs587776425
Biobank	rs587776425
1000 genomes	rs587776425
hgdp	rs587776425
ensembl	rs587776425
geneview	rs587776425
scholar	rs587776425
google	rs587776425
pharmgkb	rs587776425
gwascentral	rs587776425
openSNP	rs587776425
23andMe	rs587776425
SNPshot	rs587776425
SNPdbe	rs587776425
MSV3d	rs587776425
GWAS Ctlg	rs587776425

Max Magnitude

7

ClinVar
Risk	Rs587776425(A;A)
Alt	Rs587776425(A;A)
Reference	Rs587776425(-;-)
Significance	Pathogenic
Disease	not provided Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	not provided Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23614915dupT
CLNSRC	ClinVar
CLNACC	RCV000133487.1, RCV000195604.1, RCV000454197.1,