rs397509080

Orientation

minus

Stabilized

minus

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

Make rs397509080(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091990

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509080
dbSNP (classic)	rs397509080
ClinGen	rs397509080
ebi	rs397509080
HLI	rs397509080
Exac	rs397509080
Gnomad	rs397509080
Varsome	rs397509080
LitVar	rs397509080
Map	rs397509080
PheGenI	rs397509080
Biobank	rs397509080
1000 genomes	rs397509080
hgdp	rs397509080
ensembl	rs397509080
geneview	rs397509080
scholar	rs397509080
google	rs397509080
pharmgkb	rs397509080
gwascentral	rs397509080
openSNP	rs397509080
23andMe	rs397509080
SNPshot	rs397509080
SNPdbe	rs397509080
MSV3d	rs397509080
GWAS Ctlg	rs397509080

Max Magnitude

6

aka c.788-959_788-958del

ClinVar
Risk	rs397509080(-;-)
Alt	rs397509080(-;-)
Reference	Rs397509080(CG;CG)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244007_41244008delCG
CLNSRC	ClinVar
CLNACC	RCV000048225.2,