rs80358923

Orientation

plus

Stabilized

plus

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

Make rs80358923(C;C)

Make rs80358923(C;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32346848

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80358923
dbSNP (classic)	rs80358923
ClinGen	rs80358923
ebi	rs80358923
HLI	rs80358923
Exac	rs80358923
Gnomad	rs80358923
Varsome	rs80358923
LitVar	rs80358923
Map	rs80358923
PheGenI	rs80358923
Biobank	rs80358923
1000 genomes	rs80358923
hgdp	rs80358923
ensembl	rs80358923
geneview	rs80358923
scholar	rs80358923
google	rs80358923
pharmgkb	rs80358923
gwascentral	rs80358923
openSNP	rs80358923
23andMe	rs80358923
SNPshot	rs80358923
SNPdbe	rs80358923
MSV3d	rs80358923
GWAS Ctlg	rs80358923

Max Magnitude

6

ClinVar
Risk	rs80358923(A;A) rs80358923(C;C)
Alt	rs80358923(A;A) rs80358923(C;C)
Reference	Rs80358923(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer not provided Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not provided Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32920985T>A; NC_000013.10:g.32920985T>C
CLNSRC	ClinVar
CLNACC	RCV000082965.4, RCV000216188.1, RCV000045098.2, RCV000113679.1,