rs397508021

Orientation

plus

Stabilized

plus

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

Make rs397508021(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379508

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508021
dbSNP (classic)	rs397508021
ClinGen	rs397508021
ebi	rs397508021
HLI	rs397508021
Exac	rs397508021
Gnomad	rs397508021
Varsome	rs397508021
LitVar	rs397508021
Map	rs397508021
PheGenI	rs397508021
Biobank	rs397508021
1000 genomes	rs397508021
hgdp	rs397508021
ensembl	rs397508021
geneview	rs397508021
scholar	rs397508021
google	rs397508021
pharmgkb	rs397508021
gwascentral	rs397508021
openSNP	rs397508021
23andMe	rs397508021
SNPshot	rs397508021
SNPdbe	rs397508021
MSV3d	rs397508021
GWAS Ctlg	rs397508021

Max Magnitude

6

ClinVar
Risk	rs397508021(-;-)
Alt	rs397508021(-;-)
Reference	Rs397508021(A;A)
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.32953645delA
CLNSRC	ClinVar
CLNACC	RCV000045663.2, RCV000256733.2,