rs80358978

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs80358978(A;A)

Make rs80358978(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32356514

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80358978
dbSNP (classic)	rs80358978
ClinGen	rs80358978
ebi	rs80358978
HLI	rs80358978
Exac	rs80358978
Gnomad	rs80358978
Varsome	rs80358978
LitVar	rs80358978
Map	rs80358978
PheGenI	rs80358978
Biobank	rs80358978
1000 genomes	rs80358978
hgdp	rs80358978
ensembl	rs80358978
geneview	rs80358978
scholar	rs80358978
google	rs80358978
pharmgkb	rs80358978
gwascentral	rs80358978
openSNP	rs80358978
23andMe	rs80358978
SNPshot	rs80358978
SNPdbe	rs80358978
MSV3d	rs80358978
GWAS Ctlg	rs80358978

Max Magnitude

0

[PMID 24470074] Rare coding variants and breast cancer risk: Evaluation of susceptibility loci identified in genome-wide association studies

ClinVar
Risk	rs80358978(A;A)
Alt	rs80358978(A;A)
Reference	Rs80358978(G;G)
Significance	Other
Disease	Breast-ovarian cancer not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Neoplasm of breast
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not specified Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome Neoplasm of breast
Reversed	0
HGVS	NC_000013.10:g.32930651G>A
CLNSRC	ClinVar
CLNACC	RCV000077404.4, RCV000120359.2, RCV000164682.2, RCV000203651.2, RCV000240741.1,