rs786202439

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

23630224

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs786202439
dbSNP (classic)	rs786202439
ClinGen	rs786202439
ebi	rs786202439
HLI	rs786202439
Exac	rs786202439
Gnomad	rs786202439
Varsome	rs786202439
LitVar	rs786202439
Map	rs786202439
PheGenI	rs786202439
Biobank	rs786202439
1000 genomes	rs786202439
hgdp	rs786202439
ensembl	rs786202439
geneview	rs786202439
scholar	rs786202439
google	rs786202439
pharmgkb	rs786202439
gwascentral	rs786202439
openSNP	rs786202439
23andMe	rs786202439
SNPshot	rs786202439
SNPdbe	rs786202439
MSV3d	rs786202439
GWAS Ctlg	rs786202439

Max Magnitude

7

ClinVar
Risk	Rs786202439(T;T)
Alt	Rs786202439(T;T)
Reference	Rs786202439(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23641545C>A
CLNSRC
CLNACC	RCV000165251.1,