rs397509176

Orientation

minus

Stabilized

minus

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

Make rs397509176(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43076537

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509176
dbSNP (classic)	rs397509176
ClinGen	rs397509176
ebi	rs397509176
HLI	rs397509176
Exac	rs397509176
Gnomad	rs397509176
Varsome	rs397509176
LitVar	rs397509176
Map	rs397509176
PheGenI	rs397509176
Biobank	rs397509176
1000 genomes	rs397509176
hgdp	rs397509176
ensembl	rs397509176
geneview	rs397509176
scholar	rs397509176
google	rs397509176
pharmgkb	rs397509176
gwascentral	rs397509176
openSNP	rs397509176
23andMe	rs397509176
SNPshot	rs397509176
SNPdbe	rs397509176
MSV3d	rs397509176
GWAS Ctlg	rs397509176

Max Magnitude

6

ClinVar
Risk	rs397509176(-;-)
Alt	rs397509176(-;-)
Reference	Rs397509176(G;G)
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.41228554delC
CLNSRC	ClinVar
CLNACC	RCV000048559.2, RCV000241018.1,