rs397507678

Orientation

plus

Stabilized

plus

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

Make rs397507678(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32337996

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507678
dbSNP (classic)	rs397507678
ClinGen	rs397507678
ebi	rs397507678
HLI	rs397507678
Exac	rs397507678
Gnomad	rs397507678
Varsome	rs397507678
LitVar	rs397507678
Map	rs397507678
PheGenI	rs397507678
Biobank	rs397507678
1000 genomes	rs397507678
hgdp	rs397507678
ensembl	rs397507678
geneview	rs397507678
scholar	rs397507678
google	rs397507678
pharmgkb	rs397507678
gwascentral	rs397507678
openSNP	rs397507678
23andMe	rs397507678
SNPshot	rs397507678
SNPdbe	rs397507678
MSV3d	rs397507678
GWAS Ctlg	rs397507678

Max Magnitude

6

ClinVar
Risk	rs397507678(T;T)
Alt	rs397507678(T;T)
Reference	Rs397507678(-;-)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32912133dupT
CLNSRC	ClinVar
CLNACC	RCV000044234.2, RCV000257562.2, RCV000483680.1,