rs397509338

Orientation

minus

Stabilized

minus

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

Make rs397509338(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094603

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509338
dbSNP (classic)	rs397509338
ClinGen	rs397509338
ebi	rs397509338
HLI	rs397509338
Exac	rs397509338
Gnomad	rs397509338
Varsome	rs397509338
LitVar	rs397509338
Map	rs397509338
PheGenI	rs397509338
Biobank	rs397509338
1000 genomes	rs397509338
hgdp	rs397509338
ensembl	rs397509338
geneview	rs397509338
scholar	rs397509338
google	rs397509338
pharmgkb	rs397509338
gwascentral	rs397509338
openSNP	rs397509338
23andMe	rs397509338
SNPshot	rs397509338
SNPdbe	rs397509338
MSV3d	rs397509338
GWAS Ctlg	rs397509338

Max Magnitude

6

ClinVar
Risk	rs397509338(T;T)
Alt	rs397509338(T;T)
Reference	Rs397509338(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1 Hereditary breast and ovarian cancer syndrome
Reversed	1
HGVS	NC_000017.10:g.41246620G>A
CLNSRC	ClinVar
CLNACC	RCV000049193.2, RCV000257439.2, RCV000416963.1,