rs397509060

Orientation

minus

Stabilized

minus

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

Make rs397509060(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43092168

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509060
dbSNP (classic)	rs397509060
ClinGen	rs397509060
ebi	rs397509060
HLI	rs397509060
Exac	rs397509060
Gnomad	rs397509060
Varsome	rs397509060
LitVar	rs397509060
Map	rs397509060
PheGenI	rs397509060
Biobank	rs397509060
1000 genomes	rs397509060
hgdp	rs397509060
ensembl	rs397509060
geneview	rs397509060
scholar	rs397509060
google	rs397509060
pharmgkb	rs397509060
gwascentral	rs397509060
openSNP	rs397509060
23andMe	rs397509060
SNPshot	rs397509060
SNPdbe	rs397509060
MSV3d	rs397509060
GWAS Ctlg	rs397509060

Max Magnitude

6

aka c.788-1140_788-1136del

ClinVar
Risk	rs397509060(-;-)
Alt	rs397509060(-;-)
Reference	Rs397509060(TTAAT;TTAAT)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41244185_41244189delATTAA
CLNSRC	ClinVar
CLNACC	RCV000048165.2,