rs397509262

Orientation

minus

Stabilized

minus

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

Make rs397509262(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43051071

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397509262
dbSNP (classic)	rs397509262
ClinGen	rs397509262
ebi	rs397509262
HLI	rs397509262
Exac	rs397509262
Gnomad	rs397509262
Varsome	rs397509262
LitVar	rs397509262
Map	rs397509262
PheGenI	rs397509262
Biobank	rs397509262
1000 genomes	rs397509262
hgdp	rs397509262
ensembl	rs397509262
geneview	rs397509262
scholar	rs397509262
google	rs397509262
pharmgkb	rs397509262
gwascentral	rs397509262
openSNP	rs397509262
23andMe	rs397509262
SNPshot	rs397509262
SNPdbe	rs397509262
MSV3d	rs397509262
GWAS Ctlg	rs397509262

Max Magnitude

6

aka c.5323_5324delAT

ClinVar
Risk	rs397509262(-;-)
Alt	rs397509262(-;-)
Reference	Rs397509262(AT;AT)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41203088_41203089delAT
CLNSRC	ClinVar
CLNACC	RCV000048929.2,