rs80359190

Orientation

plus

Stabilized

plus

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

Make rs80359190(A;G)

Make rs80359190(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32380136

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80359190
dbSNP (classic)	rs80359190
ClinGen	rs80359190
ebi	rs80359190
HLI	rs80359190
Exac	rs80359190
Gnomad	rs80359190
Varsome	rs80359190
LitVar	rs80359190
Map	rs80359190
PheGenI	rs80359190
Biobank	rs80359190
1000 genomes	rs80359190
hgdp	rs80359190
ensembl	rs80359190
geneview	rs80359190
scholar	rs80359190
google	rs80359190
pharmgkb	rs80359190
gwascentral	rs80359190
openSNP	rs80359190
23andMe	rs80359190
SNPshot	rs80359190
SNPdbe	rs80359190
MSV3d	rs80359190
GWAS Ctlg	rs80359190

Max Magnitude

6

ClinVar
Risk	rs80359190(G;G) rs80359190(T;T)
Alt	rs80359190(G;G) rs80359190(T;T)
Reference	Rs80359190(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome not specified Hereditary cancer-predisposing syndrome Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome not specified Hereditary cancer-predisposing syndrome Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32954273A>G; NC_000013.10:g.32954273A>T
CLNSRC	ClinVar
CLNACC	RCV000031806.4, RCV000045756.5, RCV000212286.2, RCV000221707.1, RCV000045757.2, RCV000256545.2,