rs587782680

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/144

Chromosome

16

Position

23630102

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587782680
dbSNP (classic)	rs587782680
ClinGen	rs587782680
ebi	rs587782680
HLI	rs587782680
Exac	rs587782680
Gnomad	rs587782680
Varsome	rs587782680
LitVar	rs587782680
Map	rs587782680
PheGenI	rs587782680
Biobank	rs587782680
1000 genomes	rs587782680
hgdp	rs587782680
ensembl	rs587782680
geneview	rs587782680
scholar	rs587782680
google	rs587782680
pharmgkb	rs587782680
gwascentral	rs587782680
openSNP	rs587782680
23andMe	rs587782680
SNPshot	rs587782680
SNPdbe	rs587782680
MSV3d	rs587782680
GWAS Ctlg	rs587782680

Max Magnitude

7

ClinVar
Risk	Rs587782680(-;-)
Alt	Rs587782680(-;-)
Reference	Rs587782680(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000016.9:g.23641423delG
CLNSRC
CLNACC	RCV000132106.5, RCV000254676.1,