rs397507915

Orientation

plus

Stabilized

plus

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

Make rs397507915(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32355261

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507915
dbSNP (classic)	rs397507915
ClinGen	rs397507915
ebi	rs397507915
HLI	rs397507915
Exac	rs397507915
Gnomad	rs397507915
Varsome	rs397507915
LitVar	rs397507915
Map	rs397507915
PheGenI	rs397507915
Biobank	rs397507915
1000 genomes	rs397507915
hgdp	rs397507915
ensembl	rs397507915
geneview	rs397507915
scholar	rs397507915
google	rs397507915
pharmgkb	rs397507915
gwascentral	rs397507915
openSNP	rs397507915
23andMe	rs397507915
SNPshot	rs397507915
SNPdbe	rs397507915
MSV3d	rs397507915
GWAS Ctlg	rs397507915

Max Magnitude

6

ClinVar
Risk	rs397507915(-;-)
Alt	rs397507915(-;-)
Reference	Rs397507915(TT;TT)
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.32929398_32929399delTT
CLNSRC	ClinVar
CLNACC	RCV000045199.2, RCV000256781.2,