rs786203775

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

23622979

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs786203775
dbSNP (classic)	rs786203775
ClinGen	rs786203775
ebi	rs786203775
HLI	rs786203775
Exac	rs786203775
Gnomad	rs786203775
Varsome	rs786203775
LitVar	rs786203775
Map	rs786203775
PheGenI	rs786203775
Biobank	rs786203775
1000 genomes	rs786203775
hgdp	rs786203775
ensembl	rs786203775
geneview	rs786203775
scholar	rs786203775
google	rs786203775
pharmgkb	rs786203775
gwascentral	rs786203775
openSNP	rs786203775
23andMe	rs786203775
SNPshot	rs786203775
SNPdbe	rs786203775
MSV3d	rs786203775
GWAS Ctlg	rs786203775

Max Magnitude

7

ClinVar
Risk	Rs786203775(T;T)
Alt	Rs786203775(T;T)
Reference	Rs786203775(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast not provided
Reversed	1
HGVS	NC_000016.9:g.23634300C>A
CLNSRC
CLNACC	RCV000167226.1, RCV000227242.2, RCV000485825.1,