rs397509113

Orientation

minus

Stabilized

minus

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

Make rs397509113(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091687

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509113
ClinGen	rs397509113
ebi	rs397509113
HLI	rs397509113
Exac	rs397509113
Varsome	rs397509113
Map	rs397509113
PheGenI	rs397509113
hapmap	rs397509113
1000 genomes	rs397509113
hgdp	rs397509113
ensembl	rs397509113
gopubmed	rs397509113
geneview	rs397509113
scholar	rs397509113
google	rs397509113
pharmgkb	rs397509113
gwascentral	rs397509113
openSNP	rs397509113
23andMe	rs397509113
23andMe all	rs397509113
SNP Nexus
SNPshot	rs397509113
SNPdbe	rs397509113
MSV3d	rs397509113
GWAS Ctlg	rs397509113

Max Magnitude

6

ClinVar
Risk	rs397509113(-;-)
Alt	rs397509113(-;-)
Reference	Rs397509113(G;G)
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.41243704delC
CLNSRC	ClinVar
CLNACC	RCV000048354.2, RCV000256801.2,