rs886040290

Orientation

minus

Stabilized

minus

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

Make rs886040290(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

43099791

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs886040290
dbSNP (classic)	rs886040290
ClinGen	rs886040290
ebi	rs886040290
HLI	rs886040290
Exac	rs886040290
Gnomad	rs886040290
Varsome	rs886040290
LitVar	rs886040290
Map	rs886040290
PheGenI	rs886040290
Biobank	rs886040290
1000 genomes	rs886040290
hgdp	rs886040290
ensembl	rs886040290
geneview	rs886040290
scholar	rs886040290
google	rs886040290
pharmgkb	rs886040290
gwascentral	rs886040290
openSNP	rs886040290
23andMe	rs886040290
SNPshot	rs886040290
SNPdbe	rs886040290
MSV3d	rs886040290
GWAS Ctlg	rs886040290

Max Magnitude

6

ClinVar
Risk	rs886040290(-;-)
Alt	rs886040290(-;-)
Reference	Rs886040290(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41251808delA
CLNSRC
CLNACC	RCV000256684.2,