rs397509206

Orientation

minus

Stabilized

minus

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

Make rs397509206(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43099828

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509206
dbSNP (classic)	rs397509206
ClinGen	rs397509206
ebi	rs397509206
HLI	rs397509206
Exac	rs397509206
Gnomad	rs397509206
Varsome	rs397509206
LitVar	rs397509206
Map	rs397509206
PheGenI	rs397509206
Biobank	rs397509206
1000 genomes	rs397509206
hgdp	rs397509206
ensembl	rs397509206
geneview	rs397509206
scholar	rs397509206
google	rs397509206
pharmgkb	rs397509206
gwascentral	rs397509206
openSNP	rs397509206
23andMe	rs397509206
SNPshot	rs397509206
SNPdbe	rs397509206
MSV3d	rs397509206
GWAS Ctlg	rs397509206

Max Magnitude

6

ClinVar
Risk	rs397509206(-;-)
Alt	rs397509206(-;-)
Reference	Rs397509206(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.41251845_41251846delAG
CLNSRC	ClinVar
CLNACC	RCV000048700.2, RCV000241069.2,