rs397509205

Orientation

minus

Stabilized

minus

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

Make rs397509205(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43070984

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509205
dbSNP (classic)	rs397509205
ClinGen	rs397509205
ebi	rs397509205
HLI	rs397509205
Exac	rs397509205
Gnomad	rs397509205
Varsome	rs397509205
LitVar	rs397509205
Map	rs397509205
PheGenI	rs397509205
Biobank	rs397509205
1000 genomes	rs397509205
hgdp	rs397509205
ensembl	rs397509205
geneview	rs397509205
scholar	rs397509205
google	rs397509205
pharmgkb	rs397509205
gwascentral	rs397509205
openSNP	rs397509205
23andMe	rs397509205
SNPshot	rs397509205
SNPdbe	rs397509205
MSV3d	rs397509205
GWAS Ctlg	rs397509205

Max Magnitude

6

ClinVar
Risk	rs397509205(T;T)
Alt	rs397509205(T;T)
Reference	Rs397509205(G;G)
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.41223001C>A
CLNSRC	ClinVar
CLNACC	RCV000048694.2, RCV000241427.2,