rs397507667

Orientation

plus

Stabilized

plus

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

Make rs397507667(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337797

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507667
dbSNP (classic)	rs397507667
ClinGen	rs397507667
ebi	rs397507667
HLI	rs397507667
Exac	rs397507667
Gnomad	rs397507667
Varsome	rs397507667
LitVar	rs397507667
Map	rs397507667
PheGenI	rs397507667
Biobank	rs397507667
1000 genomes	rs397507667
hgdp	rs397507667
ensembl	rs397507667
geneview	rs397507667
scholar	rs397507667
google	rs397507667
pharmgkb	rs397507667
gwascentral	rs397507667
openSNP	rs397507667
23andMe	rs397507667
SNPshot	rs397507667
SNPdbe	rs397507667
MSV3d	rs397507667
GWAS Ctlg	rs397507667

Max Magnitude

6

ClinVar
Risk	rs397507667(T;T)
Alt	rs397507667(T;T)
Reference	Rs397507667(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.32911934C>T
CLNSRC	ClinVar
CLNACC	RCV000044194.2, RCV000256705.2,