rs397509052

Orientation

minus

Stabilized

minus

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

Make rs397509052(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092242

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509052
dbSNP (classic)	rs397509052
ClinGen	rs397509052
ebi	rs397509052
HLI	rs397509052
Exac	rs397509052
Gnomad	rs397509052
Varsome	rs397509052
LitVar	rs397509052
Map	rs397509052
PheGenI	rs397509052
Biobank	rs397509052
1000 genomes	rs397509052
hgdp	rs397509052
ensembl	rs397509052
geneview	rs397509052
scholar	rs397509052
google	rs397509052
pharmgkb	rs397509052
gwascentral	rs397509052
openSNP	rs397509052
23andMe	rs397509052
SNPshot	rs397509052
SNPdbe	rs397509052
MSV3d	rs397509052
GWAS Ctlg	rs397509052

Max Magnitude

6

rs397509052 has merged into rs80357686

ClinVar
Risk	rs397509052(-;-)
Alt	rs397509052(-;-)
Reference	Rs397509052(A;A)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244259delT
CLNSRC	ClinVar
CLNACC	RCV000048126.2,