rs786203245

Orientation

minus

Stabilized

minus

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

Reference

GRCh38.p2 38.2/146

Chromosome

16

Position

23638131

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs786203245
dbSNP (classic)	rs786203245
ClinGen	rs786203245
ebi	rs786203245
HLI	rs786203245
Exac	rs786203245
Gnomad	rs786203245
Varsome	rs786203245
LitVar	rs786203245
Map	rs786203245
PheGenI	rs786203245
Biobank	rs786203245
1000 genomes	rs786203245
hgdp	rs786203245
ensembl	rs786203245
geneview	rs786203245
scholar	rs786203245
google	rs786203245
pharmgkb	rs786203245
gwascentral	rs786203245
openSNP	rs786203245
23andMe	rs786203245
SNPshot	rs786203245
SNPdbe	rs786203245
MSV3d	rs786203245
GWAS Ctlg	rs786203245

Max Magnitude

7

ClinVar
Risk	Rs786203245(T;T)
Alt	Rs786203245(T;T)
Reference	Rs786203245(A;A)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed	1
HGVS	NC_000016.9:g.23649452T>A
CLNSRC
CLNACC	RCV000166471.3, RCV000198571.2,