rs397507356

Orientation

plus

Stabilized

plus

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

Make rs397507356(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339958

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507356
dbSNP (classic)	rs397507356
ClinGen	rs397507356
ebi	rs397507356
HLI	rs397507356
Exac	rs397507356
Gnomad	rs397507356
Varsome	rs397507356
LitVar	rs397507356
Map	rs397507356
PheGenI	rs397507356
Biobank	rs397507356
1000 genomes	rs397507356
hgdp	rs397507356
ensembl	rs397507356
geneview	rs397507356
scholar	rs397507356
google	rs397507356
pharmgkb	rs397507356
gwascentral	rs397507356
openSNP	rs397507356
23andMe	rs397507356
SNPshot	rs397507356
SNPdbe	rs397507356
MSV3d	rs397507356
GWAS Ctlg	rs397507356

Max Magnitude

6

ClinVar
Risk	rs397507356(-;-)
Alt	rs397507356(-;-)
Reference	Rs397507356(ACAG;ACAG)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32914095_32914098delACAG
CLNSRC	ClinVar
CLNACC	RCV000031559.6, RCV000456296.1,