rs397509095

Orientation

minus

Stabilized

minus

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

Make rs397509095(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091827

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509095
dbSNP (classic)	rs397509095
ClinGen	rs397509095
ebi	rs397509095
HLI	rs397509095
Exac	rs397509095
Gnomad	rs397509095
Varsome	rs397509095
LitVar	rs397509095
Map	rs397509095
PheGenI	rs397509095
Biobank	rs397509095
1000 genomes	rs397509095
hgdp	rs397509095
ensembl	rs397509095
geneview	rs397509095
scholar	rs397509095
google	rs397509095
pharmgkb	rs397509095
gwascentral	rs397509095
openSNP	rs397509095
23andMe	rs397509095
SNPshot	rs397509095
SNPdbe	rs397509095
MSV3d	rs397509095
GWAS Ctlg	rs397509095

Max Magnitude

6

ClinVar
Risk	rs397509095(-;-)
Alt	rs397509095(-;-)
Reference	Rs397509095(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.41243844delT
CLNSRC	ClinVar
CLNACC	RCV000048289.2, RCV000257069.2,