rs397509260

Orientation

minus

Stabilized

minus

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

Make rs397509260(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43051084

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509260
dbSNP (classic)	rs397509260
ClinGen	rs397509260
ebi	rs397509260
HLI	rs397509260
Exac	rs397509260
Gnomad	rs397509260
Varsome	rs397509260
LitVar	rs397509260
Map	rs397509260
PheGenI	rs397509260
Biobank	rs397509260
1000 genomes	rs397509260
hgdp	rs397509260
ensembl	rs397509260
geneview	rs397509260
scholar	rs397509260
google	rs397509260
pharmgkb	rs397509260
gwascentral	rs397509260
openSNP	rs397509260
23andMe	rs397509260
SNPshot	rs397509260
SNPdbe	rs397509260
MSV3d	rs397509260
GWAS Ctlg	rs397509260

Max Magnitude

6

rs397509260 was merged into rs80357581

ClinVar
Risk	rs397509260(G;G)
Alt	rs397509260(G;G)
Reference	Rs397509260(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41203102dupC
CLNSRC	ClinVar
CLNACC	RCV000048921.2,