rs397507943

Orientation

plus

Stabilized

plus

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

Make rs397507943(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32362601

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507943
dbSNP (classic)	rs397507943
ClinGen	rs397507943
ebi	rs397507943
HLI	rs397507943
Exac	rs397507943
Gnomad	rs397507943
Varsome	rs397507943
LitVar	rs397507943
Map	rs397507943
PheGenI	rs397507943
Biobank	rs397507943
1000 genomes	rs397507943
hgdp	rs397507943
ensembl	rs397507943
geneview	rs397507943
scholar	rs397507943
google	rs397507943
pharmgkb	rs397507943
gwascentral	rs397507943
openSNP	rs397507943
23andMe	rs397507943
SNPshot	rs397507943
SNPdbe	rs397507943
MSV3d	rs397507943
GWAS Ctlg	rs397507943

Max Magnitude

6

ClinVar
Risk	rs397507943(A;A)
Alt	rs397507943(A;A)
Reference	Rs397507943(-;-)
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.32936738dupA
CLNSRC	ClinVar
CLNACC	RCV000045338.2, RCV000225658.2,