rs876658983

Orientation

minus

Stabilized

minus

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

Make rs876658983(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

23626291

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs876658983
dbSNP (classic)	rs876658983
ClinGen	rs876658983
ebi	rs876658983
HLI	rs876658983
Exac	rs876658983
Gnomad	rs876658983
Varsome	rs876658983
LitVar	rs876658983
Map	rs876658983
PheGenI	rs876658983
Biobank	rs876658983
1000 genomes	rs876658983
hgdp	rs876658983
ensembl	rs876658983
geneview	rs876658983
scholar	rs876658983
google	rs876658983
pharmgkb	rs876658983
gwascentral	rs876658983
openSNP	rs876658983
23andMe	rs876658983
SNPshot	rs876658983
SNPdbe	rs876658983
MSV3d	rs876658983
GWAS Ctlg	rs876658983

Max Magnitude

5

ClinVar
Risk	rs876658983(A;A)
Alt	rs876658983(A;A)
Reference	Rs876658983(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000016.9:g.23637612C>T
CLNSRC
CLNACC	RCV000216899.2, RCV000478895.1,