rs397509098

Orientation

minus

Stabilized

minus

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

Make rs397509098(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091778

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509098
dbSNP (classic)	rs397509098
ClinGen	rs397509098
ebi	rs397509098
HLI	rs397509098
Exac	rs397509098
Gnomad	rs397509098
Varsome	rs397509098
LitVar	rs397509098
Map	rs397509098
PheGenI	rs397509098
Biobank	rs397509098
1000 genomes	rs397509098
hgdp	rs397509098
ensembl	rs397509098
geneview	rs397509098
scholar	rs397509098
google	rs397509098
pharmgkb	rs397509098
gwascentral	rs397509098
openSNP	rs397509098
23andMe	rs397509098
SNPshot	rs397509098
SNPdbe	rs397509098
MSV3d	rs397509098
GWAS Ctlg	rs397509098

Max Magnitude

6

ClinVar
Risk	rs397509098(A;A)
Alt	rs397509098(A;A)
Reference	Rs397509098(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.41243795A>T
CLNSRC	ClinVar
CLNACC	RCV000048312.2, RCV000257357.2,