rs587782892

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

23629949

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587782892
dbSNP (classic)	rs587782892
ClinGen	rs587782892
ebi	rs587782892
HLI	rs587782892
Exac	rs587782892
Gnomad	rs587782892
Varsome	rs587782892
LitVar	rs587782892
Map	rs587782892
PheGenI	rs587782892
Biobank	rs587782892
1000 genomes	rs587782892
hgdp	rs587782892
ensembl	rs587782892
geneview	rs587782892
scholar	rs587782892
google	rs587782892
pharmgkb	rs587782892
gwascentral	rs587782892
openSNP	rs587782892
23andMe	rs587782892
SNPshot	rs587782892
SNPdbe	rs587782892
MSV3d	rs587782892
GWAS Ctlg	rs587782892

Max Magnitude

7

ClinVar
Risk	Rs587782892(-;-)
Alt	Rs587782892(-;-)
Reference	Rs587782892(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23641270delT
CLNSRC
CLNACC	RCV000132530.2,