rs397509336

Orientation

minus

Stabilized

minus

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

Make rs397509336(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094607

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509336
dbSNP (classic)	rs397509336
ClinGen	rs397509336
ebi	rs397509336
HLI	rs397509336
Exac	rs397509336
Gnomad	rs397509336
Varsome	rs397509336
LitVar	rs397509336
Map	rs397509336
PheGenI	rs397509336
Biobank	rs397509336
1000 genomes	rs397509336
hgdp	rs397509336
ensembl	rs397509336
geneview	rs397509336
scholar	rs397509336
google	rs397509336
pharmgkb	rs397509336
gwascentral	rs397509336
openSNP	rs397509336
23andMe	rs397509336
SNPshot	rs397509336
SNPdbe	rs397509336
MSV3d	rs397509336
GWAS Ctlg	rs397509336

Max Magnitude

6

ClinVar
Risk	rs397509336(-;-)
Alt	rs397509336(-;-)
Reference	Rs397509336(C;C)
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.41246624delG
CLNSRC	ClinVar
CLNACC	RCV000049190.2, RCV000257298.2,