rs878855122

Orientation

minus

Stabilized

minus

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

Make rs878855122(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

16

Position

23638099

Gene

PALB2

is a	snp
is	mentioned by
dbSNP	rs878855122
dbSNP (classic)	rs878855122
ClinGen	rs878855122
ebi	rs878855122
HLI	rs878855122
Exac	rs878855122
Gnomad	rs878855122
Varsome	rs878855122
LitVar	rs878855122
Map	rs878855122
PheGenI	rs878855122
Biobank	rs878855122
1000 genomes	rs878855122
hgdp	rs878855122
ensembl	rs878855122
geneview	rs878855122
scholar	rs878855122
google	rs878855122
pharmgkb	rs878855122
gwascentral	rs878855122
openSNP	rs878855122
23andMe	rs878855122
SNPshot	rs878855122
SNPdbe	rs878855122
MSV3d	rs878855122
GWAS Ctlg	rs878855122

Max Magnitude

5

ClinVar
Risk	rs878855122(T;T)
Alt	rs878855122(T;T)
Reference	Rs878855122(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	PALB2
CLNDBN	Familial cancer of breast not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000016.9:g.23649420C>A
CLNSRC
CLNACC	RCV000228882.1, RCV000255635.1, RCV000454231.1,