rs397509160

Orientation

minus

Stabilized

minus

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

Make rs397509160(A;A)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43082474

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509160
dbSNP (classic)	rs397509160
ClinGen	rs397509160
ebi	rs397509160
HLI	rs397509160
Exac	rs397509160
Gnomad	rs397509160
Varsome	rs397509160
LitVar	rs397509160
Map	rs397509160
PheGenI	rs397509160
Biobank	rs397509160
1000 genomes	rs397509160
hgdp	rs397509160
ensembl	rs397509160
geneview	rs397509160
scholar	rs397509160
google	rs397509160
pharmgkb	rs397509160
gwascentral	rs397509160
openSNP	rs397509160
23andMe	rs397509160
SNPshot	rs397509160
SNPdbe	rs397509160
MSV3d	rs397509160
GWAS Ctlg	rs397509160

Max Magnitude

6

ClinVar
Risk	rs397509160(A;A)
Alt	rs397509160(A;A)
Reference	Rs397509160(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast Neoplasm of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Neoplasm of breast
Reversed	1
HGVS	NC_000017.10:g.41234491G>T
CLNSRC	ClinVar
CLNACC	RCV000048513.2, RCV000414537.1,