rs397509093

Orientation

minus

Stabilized

minus

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

Make rs397509093(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43091833

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509093
dbSNP (classic)	rs397509093
ClinGen	rs397509093
ebi	rs397509093
HLI	rs397509093
Exac	rs397509093
Gnomad	rs397509093
Varsome	rs397509093
LitVar	rs397509093
Map	rs397509093
PheGenI	rs397509093
Biobank	rs397509093
1000 genomes	rs397509093
hgdp	rs397509093
ensembl	rs397509093
geneview	rs397509093
scholar	rs397509093
google	rs397509093
pharmgkb	rs397509093
gwascentral	rs397509093
openSNP	rs397509093
23andMe	rs397509093
SNPshot	rs397509093
SNPdbe	rs397509093
MSV3d	rs397509093
GWAS Ctlg	rs397509093

Max Magnitude

6

aka c.788-804_788-801del

ClinVar
Risk	rs397509093(-;-)
Alt	rs397509093(-;-)
Reference	Rs397509093(GTAA;GTAA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41243850_41243853delTTAC
CLNSRC	ClinVar
CLNACC	RCV000048284.2,