rs397509291

Orientation

minus

Stabilized

minus

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

Make rs397509291(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43045767

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509291
dbSNP (classic)	rs397509291
ClinGen	rs397509291
ebi	rs397509291
HLI	rs397509291
Exac	rs397509291
Gnomad	rs397509291
Varsome	rs397509291
LitVar	rs397509291
Map	rs397509291
PheGenI	rs397509291
Biobank	rs397509291
1000 genomes	rs397509291
hgdp	rs397509291
ensembl	rs397509291
geneview	rs397509291
scholar	rs397509291
google	rs397509291
pharmgkb	rs397509291
gwascentral	rs397509291
openSNP	rs397509291
23andMe	rs397509291
SNPshot	rs397509291
SNPdbe	rs397509291
MSV3d	rs397509291
GWAS Ctlg	rs397509291

Max Magnitude

6

ClinVar
Risk	rs397509291(-;-)
Alt	rs397509291(-;-)
Reference	Rs397509291(C;C)
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.41197784delG
CLNSRC	ClinVar
CLNACC	RCV000049022.2, RCV000240969.2,