rs397509079

Orientation

minus

Stabilized

minus

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

Make rs397509079(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092017

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509079
dbSNP (classic)	rs397509079
ClinGen	rs397509079
ebi	rs397509079
HLI	rs397509079
Exac	rs397509079
Gnomad	rs397509079
Varsome	rs397509079
LitVar	rs397509079
Map	rs397509079
PheGenI	rs397509079
Biobank	rs397509079
1000 genomes	rs397509079
hgdp	rs397509079
ensembl	rs397509079
geneview	rs397509079
scholar	rs397509079
google	rs397509079
pharmgkb	rs397509079
gwascentral	rs397509079
openSNP	rs397509079
23andMe	rs397509079
SNPshot	rs397509079
SNPdbe	rs397509079
MSV3d	rs397509079
GWAS Ctlg	rs397509079

Max Magnitude

6

ClinVar
Risk	rs397509079(T;T)
Alt	rs397509079(T;T)
Reference	Rs397509079(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast not provided Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast not provided Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41244034C>A
CLNSRC	ClinVar
CLNACC	RCV000048221.2, RCV000236268.1, RCV000241016.2,