rs397507629

Orientation

plus

Stabilized

plus

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

Make rs397507629(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32336810

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507629
ClinGen	rs397507629
ebi	rs397507629
HLI	rs397507629
Exac	rs397507629
Varsome	rs397507629
Map	rs397507629
PheGenI	rs397507629
hapmap	rs397507629
1000 genomes	rs397507629
hgdp	rs397507629
ensembl	rs397507629
gopubmed	rs397507629
geneview	rs397507629
scholar	rs397507629
google	rs397507629
pharmgkb	rs397507629
gwascentral	rs397507629
openSNP	rs397507629
23andMe	rs397507629
23andMe all	rs397507629
SNP Nexus
SNPshot	rs397507629
SNPdbe	rs397507629
MSV3d	rs397507629
GWAS Ctlg	rs397507629

Max Magnitude

6

ClinVar
Risk	rs397507629(T;T)
Alt	rs397507629(T;T)
Reference	Rs397507629(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32910947C>T
CLNSRC	ClinVar
CLNACC	RCV000043999.2, RCV000257203.2,