rs397507645

Orientation

plus

Stabilized

plus

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

Make rs397507645(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337225

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507645
dbSNP (classic)	rs397507645
ClinGen	rs397507645
ebi	rs397507645
HLI	rs397507645
Exac	rs397507645
Gnomad	rs397507645
Varsome	rs397507645
LitVar	rs397507645
Map	rs397507645
PheGenI	rs397507645
Biobank	rs397507645
1000 genomes	rs397507645
hgdp	rs397507645
ensembl	rs397507645
geneview	rs397507645
scholar	rs397507645
google	rs397507645
pharmgkb	rs397507645
gwascentral	rs397507645
openSNP	rs397507645
23andMe	rs397507645
SNPshot	rs397507645
SNPdbe	rs397507645
MSV3d	rs397507645
GWAS Ctlg	rs397507645

Max Magnitude

6

ClinVar
Risk	rs397507645(-;-)
Alt	rs397507645(-;-)
Reference	Rs397507645(A;A)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911362delA
CLNSRC	ClinVar
CLNACC	RCV000044078.2, RCV000257652.2,