rs397509070

Orientation

minus

Stabilized

minus

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

Make rs397509070(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092063

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509070
dbSNP (classic)	rs397509070
ClinGen	rs397509070
ebi	rs397509070
HLI	rs397509070
Exac	rs397509070
Gnomad	rs397509070
Varsome	rs397509070
LitVar	rs397509070
Map	rs397509070
PheGenI	rs397509070
Biobank	rs397509070
1000 genomes	rs397509070
hgdp	rs397509070
ensembl	rs397509070
geneview	rs397509070
scholar	rs397509070
google	rs397509070
pharmgkb	rs397509070
gwascentral	rs397509070
openSNP	rs397509070
23andMe	rs397509070
SNPshot	rs397509070
SNPdbe	rs397509070
MSV3d	rs397509070
GWAS Ctlg	rs397509070

Max Magnitude

6

aka c.788-1031del

ClinVar
Risk	rs397509070(-;-)
Alt	rs397509070(-;-)
Reference	Rs397509070(T;T)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244080delA
CLNSRC	ClinVar
CLNACC	RCV000048205.2,