rs876658577

Orientation

plus

Stabilized

plus

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

Make rs876658577(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

13

Position

32333389

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs876658577
dbSNP (classic)	rs876658577
ClinGen	rs876658577
ebi	rs876658577
HLI	rs876658577
Exac	rs876658577
Gnomad	rs876658577
Varsome	rs876658577
LitVar	rs876658577
Map	rs876658577
PheGenI	rs876658577
Biobank	rs876658577
1000 genomes	rs876658577
hgdp	rs876658577
ensembl	rs876658577
geneview	rs876658577
scholar	rs876658577
google	rs876658577
pharmgkb	rs876658577
gwascentral	rs876658577
openSNP	rs876658577
23andMe	rs876658577
SNPshot	rs876658577
SNPdbe	rs876658577
MSV3d	rs876658577
GWAS Ctlg	rs876658577

Max Magnitude

6

ClinVar
Risk	rs876658577(A;A)
Alt	rs876658577(A;A)
Reference	Rs876658577(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32907526T>A
CLNSRC
CLNACC	RCV000214167.1,