rs397509007

Merged into

rs80357540

Orientation

minus

Stabilized

minus

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

Make rs397509007(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092786

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509007
dbSNP (classic)	rs397509007
ClinGen	rs397509007
ebi	rs397509007
HLI	rs397509007
Exac	rs397509007
Gnomad	rs397509007
Varsome	rs397509007
LitVar	rs397509007
Map	rs397509007
PheGenI	rs397509007
Biobank	rs397509007
1000 genomes	rs397509007
hgdp	rs397509007
ensembl	rs397509007
geneview	rs397509007
scholar	rs397509007
google	rs397509007
pharmgkb	rs397509007
gwascentral	rs397509007
openSNP	rs397509007
23andMe	rs397509007
SNPshot	rs397509007
SNPdbe	rs397509007
MSV3d	rs397509007
GWAS Ctlg	rs397509007

Status

Merged into rs80357540

Max Magnitude

6

BRCA1, c.2744_2745delCT (p.Ser915Terfs)

ClinVar
Risk
Alt
Reference	Rs397509007(CT;CT)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41244803_41244804delAG
CLNSRC	Breast Cancer Information Core (BRCA1) OMIM Allelic Variant
CLNACC	RCV000047955.2, RCV000132272.2, RCV000167766.4,