rs397509064

Orientation

minus

Stabilized

minus

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

Make rs397509064(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092115

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509064
dbSNP (classic)	rs397509064
ClinGen	rs397509064
ebi	rs397509064
HLI	rs397509064
Exac	rs397509064
Gnomad	rs397509064
Varsome	rs397509064
LitVar	rs397509064
Map	rs397509064
PheGenI	rs397509064
Biobank	rs397509064
1000 genomes	rs397509064
hgdp	rs397509064
ensembl	rs397509064
geneview	rs397509064
scholar	rs397509064
google	rs397509064
pharmgkb	rs397509064
gwascentral	rs397509064
openSNP	rs397509064
23andMe	rs397509064
SNPshot	rs397509064
SNPdbe	rs397509064
MSV3d	rs397509064
GWAS Ctlg	rs397509064

Max Magnitude

6

aka c.788-1083del

ClinVar
Risk	rs397509064(-;-)
Alt	rs397509064(-;-)
Reference	Rs397509064(G;G)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244132delC
CLNSRC	ClinVar
CLNACC	RCV000048185.2,