rs397507790

Orientation

plus

Stabilized

plus

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

Make rs397507790(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339938

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507790
dbSNP (classic)	rs397507790
ClinGen	rs397507790
ebi	rs397507790
HLI	rs397507790
Exac	rs397507790
Gnomad	rs397507790
Varsome	rs397507790
LitVar	rs397507790
Map	rs397507790
PheGenI	rs397507790
Biobank	rs397507790
1000 genomes	rs397507790
hgdp	rs397507790
ensembl	rs397507790
geneview	rs397507790
scholar	rs397507790
google	rs397507790
pharmgkb	rs397507790
gwascentral	rs397507790
openSNP	rs397507790
23andMe	rs397507790
SNPshot	rs397507790
SNPdbe	rs397507790
MSV3d	rs397507790
GWAS Ctlg	rs397507790

Max Magnitude

6

ClinVar
Risk	rs397507790(A;A)
Alt	rs397507790(A;A)
Reference	Rs397507790(-;-)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914075dupA
CLNSRC	ClinVar
CLNACC	RCV000044687.3, RCV000166213.1, RCV000241509.2,