rs80358866

Orientation

plus

Stabilized

plus

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

Make rs80358866(C;T)

Make rs80358866(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340645

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs80358866
dbSNP (classic)	rs80358866
ClinGen	rs80358866
ebi	rs80358866
HLI	rs80358866
Exac	rs80358866
Gnomad	rs80358866
Varsome	rs80358866
LitVar	rs80358866
Map	rs80358866
PheGenI	rs80358866
Biobank	rs80358866
1000 genomes	rs80358866
hgdp	rs80358866
ensembl	rs80358866
geneview	rs80358866
scholar	rs80358866
google	rs80358866
pharmgkb	rs80358866
gwascentral	rs80358866
openSNP	rs80358866
23andMe	rs80358866
SNPshot	rs80358866
SNPdbe	rs80358866
MSV3d	rs80358866
GWAS Ctlg	rs80358866

Max Magnitude

0

ClinVar
Risk	rs80358866(T;T)
Alt	rs80358866(T;T)
Reference	Rs80358866(C;C)
Significance	Other
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000013.10:g.32914782C>T
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000031613.6, RCV000044889.5, RCV000131379.3, RCV000423925.1,