rs397507285

Orientation

plus

Stabilized

plus

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

Make rs397507285(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336781

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507285
ClinGen	rs397507285
ebi	rs397507285
HLI	rs397507285
Exac	rs397507285
Varsome	rs397507285
Map	rs397507285
PheGenI	rs397507285
hapmap	rs397507285
1000 genomes	rs397507285
hgdp	rs397507285
ensembl	rs397507285
gopubmed	rs397507285
geneview	rs397507285
scholar	rs397507285
google	rs397507285
pharmgkb	rs397507285
gwascentral	rs397507285
openSNP	rs397507285
23andMe	rs397507285
23andMe all	rs397507285
SNP Nexus
SNPshot	rs397507285
SNPdbe	rs397507285
MSV3d	rs397507285
GWAS Ctlg	rs397507285

Max Magnitude

6

ClinVar
Risk	rs397507285(G;G)
Alt	rs397507285(G;G)
Reference	Rs397507285(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer not provided Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 not provided Hereditary breast and ovarian cancer syndrome
Reversed	0
HGVS	NC_000013.10:g.32910918T>G
CLNSRC	ClinVar
CLNACC	RCV000031367.4, RCV000160047.3, RCV000204854.1,