rs80359031

Orientation

plus

Stabilized

plus

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

Make rs80359031(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363190

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359031
dbSNP (classic)	rs80359031
ClinGen	rs80359031
ebi	rs80359031
HLI	rs80359031
Exac	rs80359031
Gnomad	rs80359031
Varsome	rs80359031
LitVar	rs80359031
Map	rs80359031
PheGenI	rs80359031
Biobank	rs80359031
1000 genomes	rs80359031
hgdp	rs80359031
ensembl	rs80359031
geneview	rs80359031
scholar	rs80359031
google	rs80359031
pharmgkb	rs80359031
gwascentral	rs80359031
openSNP	rs80359031
23andMe	rs80359031
SNPshot	rs80359031
SNPdbe	rs80359031
MSV3d	rs80359031
GWAS Ctlg	rs80359031

Max Magnitude

6

ClinVar
Risk	rs80359031(T;T)
Alt	rs80359031(T;T)
Reference	Rs80359031(A;A)
Significance	Other
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32937327A>T
CLNSRC	ClinVar
CLNACC	RCV000077422.5, RCV000163034.1, RCV000257984.2, RCV000484277.1,