rs397509036

Orientation

minus

Stabilized

minus

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

Make rs397509036(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092397

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509036
dbSNP (classic)	rs397509036
ClinGen	rs397509036
ebi	rs397509036
HLI	rs397509036
Exac	rs397509036
Gnomad	rs397509036
Varsome	rs397509036
LitVar	rs397509036
Map	rs397509036
PheGenI	rs397509036
Biobank	rs397509036
1000 genomes	rs397509036
hgdp	rs397509036
ensembl	rs397509036
geneview	rs397509036
scholar	rs397509036
google	rs397509036
pharmgkb	rs397509036
gwascentral	rs397509036
openSNP	rs397509036
23andMe	rs397509036
SNPshot	rs397509036
SNPdbe	rs397509036
MSV3d	rs397509036
GWAS Ctlg	rs397509036

Max Magnitude

6

aka c.788-1374_788-1365del

ClinVar
Risk	rs397509036(-;-)
Alt	rs397509036(-;-)
Reference	Rs397509036(GCAATATTAA;GCAATATTAA)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244414_41244423delTTAATATTGC
CLNSRC	ClinVar
CLNACC	RCV000048076.2,