rs397507351

Orientation

plus

Stabilized

plus

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

Make rs397507351(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339791

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507351
dbSNP (classic)	rs397507351
ClinGen	rs397507351
ebi	rs397507351
HLI	rs397507351
Exac	rs397507351
Gnomad	rs397507351
Varsome	rs397507351
LitVar	rs397507351
Map	rs397507351
PheGenI	rs397507351
Biobank	rs397507351
1000 genomes	rs397507351
hgdp	rs397507351
ensembl	rs397507351
geneview	rs397507351
scholar	rs397507351
google	rs397507351
pharmgkb	rs397507351
gwascentral	rs397507351
openSNP	rs397507351
23andMe	rs397507351
SNPshot	rs397507351
SNPdbe	rs397507351
MSV3d	rs397507351
GWAS Ctlg	rs397507351

Max Magnitude

6

ClinVar
Risk	rs397507351(-;-)
Alt	rs397507351(-;-)
Reference	Rs397507351(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32913928delA
CLNSRC	ClinVar
CLNACC	RCV000031546.4,