rs397508890

Orientation

minus

Stabilized

minus

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

Make rs397508890(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43106508

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508890
dbSNP (classic)	rs397508890
ClinGen	rs397508890
ebi	rs397508890
HLI	rs397508890
Exac	rs397508890
Gnomad	rs397508890
Varsome	rs397508890
LitVar	rs397508890
Map	rs397508890
PheGenI	rs397508890
Biobank	rs397508890
1000 genomes	rs397508890
hgdp	rs397508890
ensembl	rs397508890
geneview	rs397508890
scholar	rs397508890
google	rs397508890
pharmgkb	rs397508890
gwascentral	rs397508890
openSNP	rs397508890
23andMe	rs397508890
SNPshot	rs397508890
SNPdbe	rs397508890
MSV3d	rs397508890
GWAS Ctlg	rs397508890

Max Magnitude

6

aka c.160del

ClinVar
Risk	rs397508890(-;-)
Alt	rs397508890(-;-)
Reference	Rs397508890(C;C)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast
Reversed	1
HGVS	NC_000017.10:g.41258525delG
CLNSRC	ClinVar
CLNACC	RCV000047540.2,