rs397509076

Orientation

minus

Stabilized

minus

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

Make rs397509076(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092036

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509076
dbSNP (classic)	rs397509076
ClinGen	rs397509076
ebi	rs397509076
HLI	rs397509076
Exac	rs397509076
Gnomad	rs397509076
Varsome	rs397509076
LitVar	rs397509076
Map	rs397509076
PheGenI	rs397509076
Biobank	rs397509076
1000 genomes	rs397509076
hgdp	rs397509076
ensembl	rs397509076
geneview	rs397509076
scholar	rs397509076
google	rs397509076
pharmgkb	rs397509076
gwascentral	rs397509076
openSNP	rs397509076
23andMe	rs397509076
SNPshot	rs397509076
SNPdbe	rs397509076
MSV3d	rs397509076
GWAS Ctlg	rs397509076

Max Magnitude

6

ClinVar
Risk	rs397509076(-;-)
Alt	rs397509076(-;-)
Reference	Rs397509076(TT;TT)
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.41244053_41244054delAA
CLNSRC	ClinVar
CLNACC	RCV000048216.2, RCV000241362.2,