rs886040301

Orientation

minus

Stabilized

minus

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

Make rs886040301(-;-)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

43045734

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs886040301
dbSNP (classic)	rs886040301
ClinGen	rs886040301
ebi	rs886040301
HLI	rs886040301
Exac	rs886040301
Gnomad	rs886040301
Varsome	rs886040301
LitVar	rs886040301
Map	rs886040301
PheGenI	rs886040301
Biobank	rs886040301
1000 genomes	rs886040301
hgdp	rs886040301
ensembl	rs886040301
geneview	rs886040301
scholar	rs886040301
google	rs886040301
pharmgkb	rs886040301
gwascentral	rs886040301
openSNP	rs886040301
23andMe	rs886040301
SNPshot	rs886040301
SNPdbe	rs886040301
MSV3d	rs886040301
GWAS Ctlg	rs886040301

Max Magnitude

6

ClinVar
Risk	rs886040301(-;-)
Alt	rs886040301(-;-)
Reference	Rs886040301(C;C)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41197751delG
CLNSRC
CLNACC	RCV000257265.1,