rs397509074

Orientation

minus

Stabilized

minus

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

Make rs397509074(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092050

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509074
dbSNP (classic)	rs397509074
ClinGen	rs397509074
ebi	rs397509074
HLI	rs397509074
Exac	rs397509074
Gnomad	rs397509074
Varsome	rs397509074
LitVar	rs397509074
Map	rs397509074
PheGenI	rs397509074
Biobank	rs397509074
1000 genomes	rs397509074
hgdp	rs397509074
ensembl	rs397509074
geneview	rs397509074
scholar	rs397509074
google	rs397509074
pharmgkb	rs397509074
gwascentral	rs397509074
openSNP	rs397509074
23andMe	rs397509074
SNPshot	rs397509074
SNPdbe	rs397509074
MSV3d	rs397509074
GWAS Ctlg	rs397509074

Max Magnitude

6

aka c.788-1018delG

ClinVar
Risk	rs397509074(-;-)
Alt	rs397509074(-;-)
Reference	Rs397509074(G;G)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244067delC
CLNSRC	ClinVar
CLNACC	RCV000048212.2,