rs397507836

Orientation

plus

Stabilized

plus

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

Make rs397507836(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340623

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507836
dbSNP (classic)	rs397507836
ClinGen	rs397507836
ebi	rs397507836
HLI	rs397507836
Exac	rs397507836
Gnomad	rs397507836
Varsome	rs397507836
LitVar	rs397507836
Map	rs397507836
PheGenI	rs397507836
Biobank	rs397507836
1000 genomes	rs397507836
hgdp	rs397507836
ensembl	rs397507836
geneview	rs397507836
scholar	rs397507836
google	rs397507836
pharmgkb	rs397507836
gwascentral	rs397507836
openSNP	rs397507836
23andMe	rs397507836
SNPshot	rs397507836
SNPdbe	rs397507836
MSV3d	rs397507836
GWAS Ctlg	rs397507836

Max Magnitude

6

ClinVar
Risk	rs397507836(-;-)
Alt	rs397507836(-;-)
Reference	Rs397507836(CA;CA)
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.32914760_32914761delCA
CLNSRC	ClinVar
CLNACC	RCV000044882.2, RCV000256957.2,