rs397509026

Orientation

minus

Stabilized

minus

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

Make rs397509026(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092578

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509026
dbSNP (classic)	rs397509026
ClinGen	rs397509026
ebi	rs397509026
HLI	rs397509026
Exac	rs397509026
Gnomad	rs397509026
Varsome	rs397509026
LitVar	rs397509026
Map	rs397509026
PheGenI	rs397509026
Biobank	rs397509026
1000 genomes	rs397509026
hgdp	rs397509026
ensembl	rs397509026
geneview	rs397509026
scholar	rs397509026
google	rs397509026
pharmgkb	rs397509026
gwascentral	rs397509026
openSNP	rs397509026
23andMe	rs397509026
SNPshot	rs397509026
SNPdbe	rs397509026
MSV3d	rs397509026
GWAS Ctlg	rs397509026

Max Magnitude

6

rs397509026 has merged into rs80357627

ClinVar
Risk	rs397509026(T;T)
Alt	rs397509026(T;T)
Reference	Rs397509026(-;-)
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.41244596dupA
CLNSRC	ClinVar
CLNACC	RCV000048022.2, RCV000257438.2,