rs587780210

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

23630034

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs587780210
dbSNP (classic)	rs587780210
ClinGen	rs587780210
ebi	rs587780210
HLI	rs587780210
Exac	rs587780210
Gnomad	rs587780210
Varsome	rs587780210
LitVar	rs587780210
Map	rs587780210
PheGenI	rs587780210
Biobank	rs587780210
1000 genomes	rs587780210
hgdp	rs587780210
ensembl	rs587780210
geneview	rs587780210
scholar	rs587780210
google	rs587780210
pharmgkb	rs587780210
gwascentral	rs587780210
openSNP	rs587780210
23andMe	rs587780210
SNPshot	rs587780210
SNPdbe	rs587780210
MSV3d	rs587780210
GWAS Ctlg	rs587780210

Max Magnitude

7

ClinVar
Risk	Rs587780210(-;-)
Alt	Rs587780210(-;-)
Reference	Rs587780210(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome not provided Familial cancer of breast
Reversed	1
HGVS	NC_000016.9:g.23641355delG
CLNSRC
CLNACC	RCV000116079.3, RCV000254677.1, RCV000409069.1,