rs397507661

Orientation

plus

Stabilized

plus

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

Make rs397507661(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337622

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507661
dbSNP (classic)	rs397507661
ClinGen	rs397507661
ebi	rs397507661
HLI	rs397507661
Exac	rs397507661
Gnomad	rs397507661
Varsome	rs397507661
LitVar	rs397507661
Map	rs397507661
PheGenI	rs397507661
Biobank	rs397507661
1000 genomes	rs397507661
hgdp	rs397507661
ensembl	rs397507661
geneview	rs397507661
scholar	rs397507661
google	rs397507661
pharmgkb	rs397507661
gwascentral	rs397507661
openSNP	rs397507661
23andMe	rs397507661
SNPshot	rs397507661
SNPdbe	rs397507661
MSV3d	rs397507661
GWAS Ctlg	rs397507661

Max Magnitude

6

ClinVar
Risk	rs397507661(-;-)
Alt	rs397507661(-;-)
Reference	Rs397507661(AG;AG)
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.32911759_32911760delGA
CLNSRC	ClinVar
CLNACC	RCV000044165.2, RCV000257018.2,