rs876659359

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;T)	6	BRCA2 variant considered pathogenic for breast cancer
(T;T)	0	common in clinvar

Make rs876659359(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32332366

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876659359
dbSNP (classic)	rs876659359
ClinGen	rs876659359
ebi	rs876659359
HLI	rs876659359
Exac	rs876659359
Gnomad	rs876659359
Varsome	rs876659359
LitVar	rs876659359
Map	rs876659359
PheGenI	rs876659359
Biobank	rs876659359
1000 genomes	rs876659359
hgdp	rs876659359
ensembl	rs876659359
geneview	rs876659359
scholar	rs876659359
google	rs876659359
pharmgkb	rs876659359
gwascentral	rs876659359
openSNP	rs876659359
23andMe	rs876659359
SNPshot	rs876659359
SNPdbe	rs876659359
MSV3d	rs876659359
GWAS Ctlg	rs876659359

Max Magnitude

6

ClinVar
Risk	rs876659359(A;A)
Alt	rs876659359(A;A)
Reference	Rs876659359(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32906503T>A
CLNSRC
CLNACC	RCV000219527.1,