rs397507300

Orientation

plus

Stabilized

plus

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

Make rs397507300(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337364

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507300
dbSNP (classic)	rs397507300
ClinGen	rs397507300
ebi	rs397507300
HLI	rs397507300
Exac	rs397507300
Gnomad	rs397507300
Varsome	rs397507300
LitVar	rs397507300
Map	rs397507300
PheGenI	rs397507300
Biobank	rs397507300
1000 genomes	rs397507300
hgdp	rs397507300
ensembl	rs397507300
geneview	rs397507300
scholar	rs397507300
google	rs397507300
pharmgkb	rs397507300
gwascentral	rs397507300
openSNP	rs397507300
23andMe	rs397507300
SNPshot	rs397507300
SNPdbe	rs397507300
MSV3d	rs397507300
GWAS Ctlg	rs397507300

Max Magnitude

6

ClinVar
Risk	rs397507300(-;-)
Alt	rs397507300(-;-)
Reference	Rs397507300(CA;CA)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome Hereditary breast and ovarian cancer syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32911501_32911502delCA
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000031395.5, RCV000132309.2, RCV000232051.1, RCV000255011.1,