rs397509045

Orientation

minus

Stabilized

minus

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

Make rs397509045(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092359

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509045
dbSNP (classic)	rs397509045
ClinGen	rs397509045
ebi	rs397509045
HLI	rs397509045
Exac	rs397509045
Gnomad	rs397509045
Varsome	rs397509045
LitVar	rs397509045
Map	rs397509045
PheGenI	rs397509045
Biobank	rs397509045
1000 genomes	rs397509045
hgdp	rs397509045
ensembl	rs397509045
geneview	rs397509045
scholar	rs397509045
google	rs397509045
pharmgkb	rs397509045
gwascentral	rs397509045
openSNP	rs397509045
23andMe	rs397509045
SNPshot	rs397509045
SNPdbe	rs397509045
MSV3d	rs397509045
GWAS Ctlg	rs397509045

Max Magnitude

6

aka c.788-1330_788-1327del

ClinVar
Risk	rs397509045(-;-)
Alt	rs397509045(-;-)
Reference	Rs397509045(AGTA;AGTA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244376_41244379delTACT
CLNSRC	ClinVar
CLNACC	RCV000048091.2,