rs397507888

Orientation

plus

Stabilized

plus

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

Make rs397507888(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32346848

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507888
dbSNP (classic)	rs397507888
ClinGen	rs397507888
ebi	rs397507888
HLI	rs397507888
Exac	rs397507888
Gnomad	rs397507888
Varsome	rs397507888
LitVar	rs397507888
Map	rs397507888
PheGenI	rs397507888
Biobank	rs397507888
1000 genomes	rs397507888
hgdp	rs397507888
ensembl	rs397507888
geneview	rs397507888
scholar	rs397507888
google	rs397507888
pharmgkb	rs397507888
gwascentral	rs397507888
openSNP	rs397507888
23andMe	rs397507888
SNPshot	rs397507888
SNPdbe	rs397507888
MSV3d	rs397507888
GWAS Ctlg	rs397507888

Max Magnitude

6

ClinVar
Risk	rs397507888(-;-)
Alt	rs397507888(-;-)
Reference	Rs397507888(T;T)
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.32920985delT
CLNSRC	ClinVar
CLNACC	RCV000045099.2, RCV000256590.2,