rs397509090

Orientation

minus

Stabilized

minus

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

Make rs397509090(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091903

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509090
dbSNP (classic)	rs397509090
ClinGen	rs397509090
ebi	rs397509090
HLI	rs397509090
Exac	rs397509090
Gnomad	rs397509090
Varsome	rs397509090
LitVar	rs397509090
Map	rs397509090
PheGenI	rs397509090
Biobank	rs397509090
1000 genomes	rs397509090
hgdp	rs397509090
ensembl	rs397509090
geneview	rs397509090
scholar	rs397509090
google	rs397509090
pharmgkb	rs397509090
gwascentral	rs397509090
openSNP	rs397509090
23andMe	rs397509090
SNPshot	rs397509090
SNPdbe	rs397509090
MSV3d	rs397509090
GWAS Ctlg	rs397509090

Max Magnitude

6

ClinVar
Risk	rs397509090(-;-)
Alt	rs397509090(-;-)
Reference	Rs397509090(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.41243920delC
CLNSRC	ClinVar
CLNACC	RCV000048264.2, RCV000257349.2,