rs397507304

Orientation

plus

Stabilized

plus

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

Make rs397507304(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337537

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507304
dbSNP (classic)	rs397507304
ClinGen	rs397507304
ebi	rs397507304
HLI	rs397507304
Exac	rs397507304
Gnomad	rs397507304
Varsome	rs397507304
LitVar	rs397507304
Map	rs397507304
PheGenI	rs397507304
Biobank	rs397507304
1000 genomes	rs397507304
hgdp	rs397507304
ensembl	rs397507304
geneview	rs397507304
scholar	rs397507304
google	rs397507304
pharmgkb	rs397507304
gwascentral	rs397507304
openSNP	rs397507304
23andMe	rs397507304
SNPshot	rs397507304
SNPdbe	rs397507304
MSV3d	rs397507304
GWAS Ctlg	rs397507304

Max Magnitude

6

ClinVar
Risk	rs397507304(-;-)
Alt	rs397507304(-;-)
Reference	Rs397507304(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32911674delA
CLNSRC	ClinVar
CLNACC	RCV000031408.4,