rs397508020

Orientation

plus

Stabilized

plus

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

Make rs397508020(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379486

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508020
dbSNP (classic)	rs397508020
ClinGen	rs397508020
ebi	rs397508020
HLI	rs397508020
Exac	rs397508020
Gnomad	rs397508020
Varsome	rs397508020
LitVar	rs397508020
Map	rs397508020
PheGenI	rs397508020
Biobank	rs397508020
1000 genomes	rs397508020
hgdp	rs397508020
ensembl	rs397508020
geneview	rs397508020
scholar	rs397508020
google	rs397508020
pharmgkb	rs397508020
gwascentral	rs397508020
openSNP	rs397508020
23andMe	rs397508020
SNPshot	rs397508020
SNPdbe	rs397508020
MSV3d	rs397508020
GWAS Ctlg	rs397508020

Max Magnitude

6

ClinVar
Risk	rs397508020(-;-)
Alt	rs397508020(-;-)
Reference	Rs397508020(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.32953623delT
CLNSRC	ClinVar
CLNACC	RCV000045659.2, RCV000257521.2,