rs397509137

Orientation

minus

Stabilized

minus

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

Make rs397509137(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091438

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509137
dbSNP (classic)	rs397509137
ClinGen	rs397509137
ebi	rs397509137
HLI	rs397509137
Exac	rs397509137
Gnomad	rs397509137
Varsome	rs397509137
LitVar	rs397509137
Map	rs397509137
PheGenI	rs397509137
Biobank	rs397509137
1000 genomes	rs397509137
hgdp	rs397509137
ensembl	rs397509137
geneview	rs397509137
scholar	rs397509137
google	rs397509137
pharmgkb	rs397509137
gwascentral	rs397509137
openSNP	rs397509137
23andMe	rs397509137
SNPshot	rs397509137
SNPdbe	rs397509137
MSV3d	rs397509137
GWAS Ctlg	rs397509137

Max Magnitude

6

ClinVar
Risk	rs397509137(-;-)
Alt	rs397509137(-;-)
Reference	Rs397509137(CT;CT)
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.41243455_41243456delAG
CLNSRC	ClinVar
CLNACC	RCV000048439.2, RCV000257689.2,