rs397508935

Orientation

minus

Stabilized

minus

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

Make rs397508935(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093465

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508935
dbSNP (classic)	rs397508935
ClinGen	rs397508935
ebi	rs397508935
HLI	rs397508935
Exac	rs397508935
Gnomad	rs397508935
Varsome	rs397508935
LitVar	rs397508935
Map	rs397508935
PheGenI	rs397508935
Biobank	rs397508935
1000 genomes	rs397508935
hgdp	rs397508935
ensembl	rs397508935
geneview	rs397508935
scholar	rs397508935
google	rs397508935
pharmgkb	rs397508935
gwascentral	rs397508935
openSNP	rs397508935
23andMe	rs397508935
SNPshot	rs397508935
SNPdbe	rs397508935
MSV3d	rs397508935
GWAS Ctlg	rs397508935

Max Magnitude

6

ClinVar
Risk	rs397508935(-;-)
Alt	rs397508935(-;-)
Reference	Rs397508935(CAAG;CAAG)
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.41245482_41245485delCTTG
CLNSRC	ClinVar
CLNACC	RCV000047697.2, RCV000257753.2,