rs397509041

Orientation

minus

Stabilized

minus

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

Make rs397509041(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092374

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509041
dbSNP (classic)	rs397509041
ClinGen	rs397509041
ebi	rs397509041
HLI	rs397509041
Exac	rs397509041
Gnomad	rs397509041
Varsome	rs397509041
LitVar	rs397509041
Map	rs397509041
PheGenI	rs397509041
Biobank	rs397509041
1000 genomes	rs397509041
hgdp	rs397509041
ensembl	rs397509041
geneview	rs397509041
scholar	rs397509041
google	rs397509041
pharmgkb	rs397509041
gwascentral	rs397509041
openSNP	rs397509041
23andMe	rs397509041
SNPshot	rs397509041
SNPdbe	rs397509041
MSV3d	rs397509041
GWAS Ctlg	rs397509041

Max Magnitude

6

aka c.788-1342del

ClinVar
Risk	rs397509041(-;-)
Alt	rs397509041(-;-)
Reference	Rs397509041(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.41244391delC
CLNSRC	ClinVar
CLNACC	RCV000048086.2,