rs397508908

Orientation

minus

Stabilized

minus

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

Make rs397508908(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093726

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508908
ClinGen	rs397508908
ebi	rs397508908
HLI	rs397508908
Exac	rs397508908
Varsome	rs397508908
Map	rs397508908
PheGenI	rs397508908
hapmap	rs397508908
1000 genomes	rs397508908
hgdp	rs397508908
ensembl	rs397508908
gopubmed	rs397508908
geneview	rs397508908
scholar	rs397508908
google	rs397508908
pharmgkb	rs397508908
gwascentral	rs397508908
openSNP	rs397508908
23andMe	rs397508908
23andMe all	rs397508908
SNP Nexus
SNPshot	rs397508908
SNPdbe	rs397508908
MSV3d	rs397508908
GWAS Ctlg	rs397508908

Max Magnitude

6

ClinVar
Risk	rs397508908(-;-)
Alt	rs397508908(-;-)
Reference	Rs397508908(A;A)
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.41245743delT
CLNSRC	ClinVar
CLNACC	RCV000047591.2, RCV000257371.2,