rs876658166

Orientation

minus

Stabilized

minus

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

Make rs876658166(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

23635168

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs876658166
dbSNP (classic)	rs876658166
ClinGen	rs876658166
ebi	rs876658166
HLI	rs876658166
Exac	rs876658166
Gnomad	rs876658166
Varsome	rs876658166
LitVar	rs876658166
Map	rs876658166
PheGenI	rs876658166
Biobank	rs876658166
1000 genomes	rs876658166
hgdp	rs876658166
ensembl	rs876658166
geneview	rs876658166
scholar	rs876658166
google	rs876658166
pharmgkb	rs876658166
gwascentral	rs876658166
openSNP	rs876658166
23andMe	rs876658166
SNPshot	rs876658166
SNPdbe	rs876658166
MSV3d	rs876658166
GWAS Ctlg	rs876658166

Max Magnitude

5

ClinVar
Risk	rs876658166(T;T)
Alt	rs876658166(T;T)
Reference	Rs876658166(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23646489G>A
CLNSRC
CLNACC	RCV000222117.1,