rs397509077

Orientation

minus

Stabilized

minus

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

Make rs397509077(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092027

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509077
dbSNP (classic)	rs397509077
ClinGen	rs397509077
ebi	rs397509077
HLI	rs397509077
Exac	rs397509077
Gnomad	rs397509077
Varsome	rs397509077
LitVar	rs397509077
Map	rs397509077
PheGenI	rs397509077
Biobank	rs397509077
1000 genomes	rs397509077
hgdp	rs397509077
ensembl	rs397509077
geneview	rs397509077
scholar	rs397509077
google	rs397509077
pharmgkb	rs397509077
gwascentral	rs397509077
openSNP	rs397509077
23andMe	rs397509077
SNPshot	rs397509077
SNPdbe	rs397509077
MSV3d	rs397509077
GWAS Ctlg	rs397509077

Max Magnitude

6

rs397509077 has merged into rs397507216

ClinVar
Risk	rs397509077(A;A)
Alt	rs397509077(A;A)
Reference	Rs397509077(-;-)
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.41244045dupT
CLNSRC	ClinVar
CLNACC	RCV000048218.2, RCV000410675.1,