rs397508945

Orientation

minus

Stabilized

minus

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

Make rs397508945(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093354

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508945
dbSNP (classic)	rs397508945
ClinGen	rs397508945
ebi	rs397508945
HLI	rs397508945
Exac	rs397508945
Gnomad	rs397508945
Varsome	rs397508945
LitVar	rs397508945
Map	rs397508945
PheGenI	rs397508945
Biobank	rs397508945
1000 genomes	rs397508945
hgdp	rs397508945
ensembl	rs397508945
geneview	rs397508945
scholar	rs397508945
google	rs397508945
pharmgkb	rs397508945
gwascentral	rs397508945
openSNP	rs397508945
23andMe	rs397508945
SNPshot	rs397508945
SNPdbe	rs397508945
MSV3d	rs397508945
GWAS Ctlg	rs397508945

Max Magnitude

6

ClinVar
Risk	rs397508945(-;-)
Alt	rs397508945(-;-)
Reference	Rs397508945(CT;CT)
Significance	Pathogenic
Disease	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Hereditary breast and ovarian cancer syndrome Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41245371_41245372delAG
CLNSRC	ClinVar
CLNACC	RCV000047743.3, RCV000257838.2,