rs397509240

Orientation

minus

Stabilized

minus

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

Make rs397509240(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43057099

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509240
dbSNP (classic)	rs397509240
ClinGen	rs397509240
ebi	rs397509240
HLI	rs397509240
Exac	rs397509240
Gnomad	rs397509240
Varsome	rs397509240
LitVar	rs397509240
Map	rs397509240
PheGenI	rs397509240
Biobank	rs397509240
1000 genomes	rs397509240
hgdp	rs397509240
ensembl	rs397509240
geneview	rs397509240
scholar	rs397509240
google	rs397509240
pharmgkb	rs397509240
gwascentral	rs397509240
openSNP	rs397509240
23andMe	rs397509240
SNPshot	rs397509240
SNPdbe	rs397509240
MSV3d	rs397509240
GWAS Ctlg	rs397509240

Max Magnitude

6

BRCA1, c.5230delA (p.Arg1744Glufs)

ClinVar
Risk	rs397509240(-;-)
Alt	rs397509240(-;-)
Reference	Rs397509240(A;A)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41209116delT
CLNSRC	ClinVar
CLNACC	RCV000048872.2, RCV000217310.1,