rs752592662

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;C)	5	PALB2-related cancer risk

Make rs752592662(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

23630046

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs752592662
dbSNP (classic)	rs752592662
ClinGen	rs752592662
ebi	rs752592662
HLI	rs752592662
Exac	rs752592662
Gnomad	rs752592662
Varsome	rs752592662
LitVar	rs752592662
Map	rs752592662
PheGenI	rs752592662
Biobank	rs752592662
1000 genomes	rs752592662
hgdp	rs752592662
ensembl	rs752592662
geneview	rs752592662
scholar	rs752592662
google	rs752592662
pharmgkb	rs752592662
gwascentral	rs752592662
openSNP	rs752592662
23andMe	rs752592662
SNPshot	rs752592662
SNPdbe	rs752592662
MSV3d	rs752592662
GWAS Ctlg	rs752592662

Max Magnitude

5

ClinVar
Risk	rs752592662(C;C)
Alt	rs752592662(C;C)
Reference	Rs752592662(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000016.9:g.23641367A>C
CLNSRC
CLNACC	RCV000223583.1,