rs397507637

Orientation

plus

Stabilized

plus

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

Make rs397507637(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337056

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507637
dbSNP (classic)	rs397507637
ClinGen	rs397507637
ebi	rs397507637
HLI	rs397507637
Exac	rs397507637
Gnomad	rs397507637
Varsome	rs397507637
LitVar	rs397507637
Map	rs397507637
PheGenI	rs397507637
Biobank	rs397507637
1000 genomes	rs397507637
hgdp	rs397507637
ensembl	rs397507637
geneview	rs397507637
scholar	rs397507637
google	rs397507637
pharmgkb	rs397507637
gwascentral	rs397507637
openSNP	rs397507637
23andMe	rs397507637
SNPshot	rs397507637
SNPdbe	rs397507637
MSV3d	rs397507637
GWAS Ctlg	rs397507637

Max Magnitude

6

ClinVar
Risk	rs397507637(-;-)
Alt	rs397507637(-;-)
Reference	Rs397507637(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32911193delC
CLNSRC	ClinVar
CLNACC	RCV000044042.3, RCV000241251.2, RCV000456130.1,