rs397509115

Orientation

minus

Stabilized

minus

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

Make rs397509115(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091655

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509115
dbSNP (classic)	rs397509115
ClinGen	rs397509115
ebi	rs397509115
HLI	rs397509115
Exac	rs397509115
Gnomad	rs397509115
Varsome	rs397509115
LitVar	rs397509115
Map	rs397509115
PheGenI	rs397509115
Biobank	rs397509115
1000 genomes	rs397509115
hgdp	rs397509115
ensembl	rs397509115
geneview	rs397509115
scholar	rs397509115
google	rs397509115
pharmgkb	rs397509115
gwascentral	rs397509115
openSNP	rs397509115
23andMe	rs397509115
SNPshot	rs397509115
SNPdbe	rs397509115
MSV3d	rs397509115
GWAS Ctlg	rs397509115

Max Magnitude

6

aka c.788-623del

ClinVar
Risk	rs397509115(-;-)
Alt	rs397509115(-;-)
Reference	Rs397509115(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.41243672delA
CLNSRC	ClinVar
CLNACC	RCV000048364.2,