rs397507818

Orientation

plus

Stabilized

plus

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

Make rs397507818(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340339

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507818
dbSNP (classic)	rs397507818
ClinGen	rs397507818
ebi	rs397507818
HLI	rs397507818
Exac	rs397507818
Gnomad	rs397507818
Varsome	rs397507818
LitVar	rs397507818
Map	rs397507818
PheGenI	rs397507818
Biobank	rs397507818
1000 genomes	rs397507818
hgdp	rs397507818
ensembl	rs397507818
geneview	rs397507818
scholar	rs397507818
google	rs397507818
pharmgkb	rs397507818
gwascentral	rs397507818
openSNP	rs397507818
23andMe	rs397507818
SNPshot	rs397507818
SNPdbe	rs397507818
MSV3d	rs397507818
GWAS Ctlg	rs397507818

Max Magnitude

6

ClinVar
Risk	rs397507818(A;A)
Alt	rs397507818(A;A)
Reference	Rs397507818(-;-)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914476dupA
CLNSRC	ClinVar
CLNACC	RCV000044812.3, RCV000257511.2,