rs80359774

Orientation

plus

Stabilized

plus

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

Make rs80359774(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32398189

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359774
dbSNP (classic)	rs80359774
ClinGen	rs80359774
ebi	rs80359774
HLI	rs80359774
Exac	rs80359774
Gnomad	rs80359774
Varsome	rs80359774
LitVar	rs80359774
Map	rs80359774
PheGenI	rs80359774
Biobank	rs80359774
1000 genomes	rs80359774
hgdp	rs80359774
ensembl	rs80359774
geneview	rs80359774
scholar	rs80359774
google	rs80359774
pharmgkb	rs80359774
gwascentral	rs80359774
openSNP	rs80359774
23andMe	rs80359774
SNPshot	rs80359774
SNPdbe	rs80359774
MSV3d	rs80359774
GWAS Ctlg	rs80359774

Max Magnitude

6

ClinVar
Risk	rs80359774(-;-)
Alt	rs80359774(-;-)
Reference	Rs80359774(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32972326delT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000045884.2, RCV000114152.3, RCV000482822.1,