rs397509261

Orientation

minus

Stabilized

minus

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

Make rs397509261(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43051080

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509261
dbSNP (classic)	rs397509261
ClinGen	rs397509261
ebi	rs397509261
HLI	rs397509261
Exac	rs397509261
Gnomad	rs397509261
Varsome	rs397509261
LitVar	rs397509261
Map	rs397509261
PheGenI	rs397509261
Biobank	rs397509261
1000 genomes	rs397509261
hgdp	rs397509261
ensembl	rs397509261
geneview	rs397509261
scholar	rs397509261
google	rs397509261
pharmgkb	rs397509261
gwascentral	rs397509261
openSNP	rs397509261
23andMe	rs397509261
SNPshot	rs397509261
SNPdbe	rs397509261
MSV3d	rs397509261
GWAS Ctlg	rs397509261

Max Magnitude

6

ClinVar
Risk	rs397509261(-;-)
Alt	rs397509261(-;-)
Reference	Rs397509261(T;T)
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.41203097delA
CLNSRC	ClinVar
CLNACC	RCV000048924.2, RCV000257542.1,