rs397507410

Orientation

plus

Stabilized

plus

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

Make rs397507410(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32376717

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507410
dbSNP (classic)	rs397507410
ClinGen	rs397507410
ebi	rs397507410
HLI	rs397507410
Exac	rs397507410
Gnomad	rs397507410
Varsome	rs397507410
LitVar	rs397507410
Map	rs397507410
PheGenI	rs397507410
Biobank	rs397507410
1000 genomes	rs397507410
hgdp	rs397507410
ensembl	rs397507410
geneview	rs397507410
scholar	rs397507410
google	rs397507410
pharmgkb	rs397507410
gwascentral	rs397507410
openSNP	rs397507410
23andMe	rs397507410
SNPshot	rs397507410
SNPdbe	rs397507410
MSV3d	rs397507410
GWAS Ctlg	rs397507410

Max Magnitude

6

ClinVar
Risk	rs397507410(-;-)
Alt	rs397507410(-;-)
Reference	Rs397507410(C;C)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32950854delC
CLNSRC	ClinVar
CLNACC	RCV000031761.5, RCV000219473.1, RCV000476800.1,