rs397509141

Orientation

minus

Stabilized

minus

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

Make rs397509141(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43090992

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509141
ClinGen	rs397509141
ebi	rs397509141
HLI	rs397509141
Exac	rs397509141
Varsome	rs397509141
Map	rs397509141
PheGenI	rs397509141
hapmap	rs397509141
1000 genomes	rs397509141
hgdp	rs397509141
ensembl	rs397509141
gopubmed	rs397509141
geneview	rs397509141
scholar	rs397509141
google	rs397509141
pharmgkb	rs397509141
gwascentral	rs397509141
openSNP	rs397509141
23andMe	rs397509141
23andMe all	rs397509141
SNP Nexus
SNPshot	rs397509141
SNPdbe	rs397509141
MSV3d	rs397509141
GWAS Ctlg	rs397509141

Max Magnitude

6

ClinVar
Risk	rs397509141(-;-)
Alt	rs397509141(-;-)
Reference	Rs397509141(CT;CT)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer not provided
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1 not provided
Reversed	1
HGVS	NC_000017.10:g.41243009_41243010delAG
CLNSRC	ClinVar
CLNACC	RCV000048457.2, RCV000239228.2, RCV000486895.1,