rs397509038

Orientation

minus

Stabilized

minus

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

Make rs397509038(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092386

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509038
dbSNP (classic)	rs397509038
ClinGen	rs397509038
ebi	rs397509038
HLI	rs397509038
Exac	rs397509038
Gnomad	rs397509038
Varsome	rs397509038
LitVar	rs397509038
Map	rs397509038
PheGenI	rs397509038
Biobank	rs397509038
1000 genomes	rs397509038
hgdp	rs397509038
ensembl	rs397509038
geneview	rs397509038
scholar	rs397509038
google	rs397509038
pharmgkb	rs397509038
gwascentral	rs397509038
openSNP	rs397509038
23andMe	rs397509038
SNPshot	rs397509038
SNPdbe	rs397509038
MSV3d	rs397509038
GWAS Ctlg	rs397509038

Max Magnitude

6

ClinVar
Risk	rs397509038(-;-)
Alt	rs397509038(-;-)
Reference	Rs397509038(T;T)
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.41244403delA
CLNSRC	ClinVar
CLNACC	RCV000048082.2, RCV000256523.2,