rs397509110

Orientation

minus

Stabilized

minus

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

Make rs397509110(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091711

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509110
dbSNP (classic)	rs397509110
ClinGen	rs397509110
ebi	rs397509110
HLI	rs397509110
Exac	rs397509110
Gnomad	rs397509110
Varsome	rs397509110
LitVar	rs397509110
Map	rs397509110
PheGenI	rs397509110
Biobank	rs397509110
1000 genomes	rs397509110
hgdp	rs397509110
ensembl	rs397509110
geneview	rs397509110
scholar	rs397509110
google	rs397509110
pharmgkb	rs397509110
gwascentral	rs397509110
openSNP	rs397509110
23andMe	rs397509110
SNPshot	rs397509110
SNPdbe	rs397509110
MSV3d	rs397509110
GWAS Ctlg	rs397509110

Max Magnitude

6

ClinVar
Risk	rs397509110(-;-)
Alt	rs397509110(-;-)
Reference	Rs397509110(G;G)
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.41243728delC
CLNSRC	ClinVar
CLNACC	RCV000048343.2, RCV000256600.2,