rs397507573

Orientation

plus

Stabilized

plus

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

Make rs397507573(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32319124

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507573
ClinGen	rs397507573
ebi	rs397507573
HLI	rs397507573
Exac	rs397507573
Varsome	rs397507573
Map	rs397507573
PheGenI	rs397507573
hapmap	rs397507573
1000 genomes	rs397507573
hgdp	rs397507573
ensembl	rs397507573
gopubmed	rs397507573
geneview	rs397507573
scholar	rs397507573
google	rs397507573
pharmgkb	rs397507573
gwascentral	rs397507573
openSNP	rs397507573
23andMe	rs397507573
23andMe all	rs397507573
SNP Nexus
SNPshot	rs397507573
SNPdbe	rs397507573
MSV3d	rs397507573
GWAS Ctlg	rs397507573

Max Magnitude

6

ClinVar
Risk	rs397507573(-;-)
Alt	rs397507573(-;-)
Reference	Rs397507573(G;G)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32893261delG
CLNSRC	ClinVar
CLNACC	RCV000043749.3, RCV000241066.2, RCV000483184.1,