rs397508019

Orientation

plus

Stabilized

plus

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

Make rs397508019(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379477

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508019
dbSNP (classic)	rs397508019
ClinGen	rs397508019
ebi	rs397508019
HLI	rs397508019
Exac	rs397508019
Gnomad	rs397508019
Varsome	rs397508019
LitVar	rs397508019
Map	rs397508019
PheGenI	rs397508019
Biobank	rs397508019
1000 genomes	rs397508019
hgdp	rs397508019
ensembl	rs397508019
geneview	rs397508019
scholar	rs397508019
google	rs397508019
pharmgkb	rs397508019
gwascentral	rs397508019
openSNP	rs397508019
23andMe	rs397508019
SNPshot	rs397508019
SNPdbe	rs397508019
MSV3d	rs397508019
GWAS Ctlg	rs397508019

Max Magnitude

6

ClinVar
Risk	rs397508019(-;-)
Alt	rs397508019(-;-)
Reference	Rs397508019(T;T)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32953614delT
CLNSRC	ClinVar
CLNACC	RCV000045655.3, RCV000257384.2,