rs397509103

Orientation

minus

Stabilized

minus

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

Make rs397509103(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091767

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509103
dbSNP (classic)	rs397509103
ClinGen	rs397509103
ebi	rs397509103
HLI	rs397509103
Exac	rs397509103
Gnomad	rs397509103
Varsome	rs397509103
LitVar	rs397509103
Map	rs397509103
PheGenI	rs397509103
Biobank	rs397509103
1000 genomes	rs397509103
hgdp	rs397509103
ensembl	rs397509103
geneview	rs397509103
scholar	rs397509103
google	rs397509103
pharmgkb	rs397509103
gwascentral	rs397509103
openSNP	rs397509103
23andMe	rs397509103
SNPshot	rs397509103
SNPdbe	rs397509103
MSV3d	rs397509103
GWAS Ctlg	rs397509103

Max Magnitude

6

ClinVar
Risk	rs397509103(-;-)
Alt	rs397509103(-;-)
Reference	Rs397509103(AA;AA)
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.41243784_41243785delTT
CLNSRC	ClinVar
CLNACC	RCV000048323.2, RCV000257218.1,