rs397508899

Orientation

minus

Stabilized

minus

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

Make rs397508899(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43093831

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508899
dbSNP (classic)	rs397508899
ClinGen	rs397508899
ebi	rs397508899
HLI	rs397508899
Exac	rs397508899
Gnomad	rs397508899
Varsome	rs397508899
LitVar	rs397508899
Map	rs397508899
PheGenI	rs397508899
Biobank	rs397508899
1000 genomes	rs397508899
hgdp	rs397508899
ensembl	rs397508899
geneview	rs397508899
scholar	rs397508899
google	rs397508899
pharmgkb	rs397508899
gwascentral	rs397508899
openSNP	rs397508899
23andMe	rs397508899
SNPshot	rs397508899
SNPdbe	rs397508899
MSV3d	rs397508899
GWAS Ctlg	rs397508899

Max Magnitude

6

rs397508899 has merged into rs80357784

ClinVar
Risk	rs397508899(-;-)
Alt	rs397508899(-;-)
Reference	Rs397508899(A;A)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41245848delT
CLNSRC	ClinVar
CLNACC	RCV000047562.2,