rs80359772

Orientation

plus

Stabilized

plus

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

Make rs80359772(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32398179

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359772
dbSNP (classic)	rs80359772
ClinGen	rs80359772
ebi	rs80359772
HLI	rs80359772
Exac	rs80359772
Gnomad	rs80359772
Varsome	rs80359772
LitVar	rs80359772
Map	rs80359772
PheGenI	rs80359772
Biobank	rs80359772
1000 genomes	rs80359772
hgdp	rs80359772
ensembl	rs80359772
geneview	rs80359772
scholar	rs80359772
google	rs80359772
pharmgkb	rs80359772
gwascentral	rs80359772
openSNP	rs80359772
23andMe	rs80359772
SNPshot	rs80359772
SNPdbe	rs80359772
MSV3d	rs80359772
GWAS Ctlg	rs80359772

Max Magnitude

6

ClinVar
Risk	rs80359772(-;-)
Alt	rs80359772(-;-)
Reference	Rs80359772(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32972316delT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045883.2, RCV000114150.3, RCV000130019.3,