rs397507959

Orientation

plus

Stabilized

plus

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

Make rs397507959(A;A)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363255

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507959
dbSNP (classic)	rs397507959
ClinGen	rs397507959
ebi	rs397507959
HLI	rs397507959
Exac	rs397507959
Gnomad	rs397507959
Varsome	rs397507959
LitVar	rs397507959
Map	rs397507959
PheGenI	rs397507959
Biobank	rs397507959
1000 genomes	rs397507959
hgdp	rs397507959
ensembl	rs397507959
geneview	rs397507959
scholar	rs397507959
google	rs397507959
pharmgkb	rs397507959
gwascentral	rs397507959
openSNP	rs397507959
23andMe	rs397507959
SNPshot	rs397507959
SNPdbe	rs397507959
MSV3d	rs397507959
GWAS Ctlg	rs397507959

Max Magnitude

6

ClinVar
Risk	rs397507959(A;A)
Alt	rs397507959(A;A)
Reference	Rs397507959(-;-)
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.32937392dupA
CLNSRC	ClinVar
CLNACC	RCV000045403.3, RCV000241379.1,