rs397509013

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;TAAG)	6	BRCA1 variant considered pathogenic for breast cancer
(TAAG;TAAG)	0	common in clinvar

Make rs397509013(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092720

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509013
dbSNP (classic)	rs397509013
ClinGen	rs397509013
ebi	rs397509013
HLI	rs397509013
Exac	rs397509013
Gnomad	rs397509013
Varsome	rs397509013
LitVar	rs397509013
Map	rs397509013
PheGenI	rs397509013
Biobank	rs397509013
1000 genomes	rs397509013
hgdp	rs397509013
ensembl	rs397509013
geneview	rs397509013
scholar	rs397509013
google	rs397509013
pharmgkb	rs397509013
gwascentral	rs397509013
openSNP	rs397509013
23andMe	rs397509013
SNPshot	rs397509013
SNPdbe	rs397509013
MSV3d	rs397509013
GWAS Ctlg	rs397509013

Max Magnitude

6

ClinVar
Risk	rs397509013(-;-)
Alt	rs397509013(-;-)
Reference	Rs397509013(TAAG;TAAG)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41244737_41244740delCTTA
CLNSRC	ClinVar
CLNACC	RCV000047976.2, RCV000257883.2,