rs80358766

Orientation

plus

Stabilized

plus

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

Make rs80358766(A;A)

Make rs80358766(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339783

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80358766
dbSNP (classic)	rs80358766
ClinGen	rs80358766
ebi	rs80358766
HLI	rs80358766
Exac	rs80358766
Gnomad	rs80358766
Varsome	rs80358766
LitVar	rs80358766
Map	rs80358766
PheGenI	rs80358766
Biobank	rs80358766
1000 genomes	rs80358766
hgdp	rs80358766
ensembl	rs80358766
geneview	rs80358766
scholar	rs80358766
google	rs80358766
pharmgkb	rs80358766
gwascentral	rs80358766
openSNP	rs80358766
23andMe	rs80358766
SNPshot	rs80358766
SNPdbe	rs80358766
MSV3d	rs80358766
GWAS Ctlg	rs80358766

Max Magnitude

0

ClinVar
Risk	rs80358766(A;A)
Alt	rs80358766(A;A)
Reference	Rs80358766(G;G)
Significance	Other
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000013.10:g.32913920G>A
CLNSRC	ClinVar
CLNACC	RCV000044658.4, RCV000077352.6, RCV000214539.1, RCV000219100.1,