rs587782232

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.p2 38.2/144

Chromosome

16

Position

23635695

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587782232
dbSNP (classic)	rs587782232
ClinGen	rs587782232
ebi	rs587782232
HLI	rs587782232
Exac	rs587782232
Gnomad	rs587782232
Varsome	rs587782232
LitVar	rs587782232
Map	rs587782232
PheGenI	rs587782232
Biobank	rs587782232
1000 genomes	rs587782232
hgdp	rs587782232
ensembl	rs587782232
geneview	rs587782232
scholar	rs587782232
google	rs587782232
pharmgkb	rs587782232
gwascentral	rs587782232
openSNP	rs587782232
23andMe	rs587782232
SNPshot	rs587782232
SNPdbe	rs587782232
MSV3d	rs587782232
GWAS Ctlg	rs587782232

Max Magnitude

7

ClinVar
Risk	Rs587782232(A;A)
Alt	Rs587782232(A;A)
Reference	Rs587782232(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23647017dupT
CLNSRC
CLNACC	RCV000130929.2,