rs397509119

Orientation

minus

Stabilized

minus

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

Make rs397509119(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091605

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509119
dbSNP (classic)	rs397509119
ClinGen	rs397509119
ebi	rs397509119
HLI	rs397509119
Exac	rs397509119
Gnomad	rs397509119
Varsome	rs397509119
LitVar	rs397509119
Map	rs397509119
PheGenI	rs397509119
Biobank	rs397509119
1000 genomes	rs397509119
hgdp	rs397509119
ensembl	rs397509119
geneview	rs397509119
scholar	rs397509119
google	rs397509119
pharmgkb	rs397509119
gwascentral	rs397509119
openSNP	rs397509119
23andMe	rs397509119
SNPshot	rs397509119
SNPdbe	rs397509119
MSV3d	rs397509119
GWAS Ctlg	rs397509119

Max Magnitude

6

ClinVar
Risk	rs397509119(-;-)
Alt	rs397509119(-;-)
Reference	Rs397509119(A;A)
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.41243622delT
CLNSRC	ClinVar
CLNACC	RCV000048381.2, RCV000257479.2,