rs80358155

Orientation

minus

Stabilized

minus

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

Make rs80358155(C;C)

Reference

GRCh38 38.1/142

Chromosome

17

Position

43099882

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs80358155
dbSNP (classic)	rs80358155
ClinGen	rs80358155
ebi	rs80358155
HLI	rs80358155
Exac	rs80358155
Gnomad	rs80358155
Varsome	rs80358155
LitVar	rs80358155
Map	rs80358155
PheGenI	rs80358155
Biobank	rs80358155
1000 genomes	rs80358155
hgdp	rs80358155
ensembl	rs80358155
geneview	rs80358155
scholar	rs80358155
google	rs80358155
pharmgkb	rs80358155
gwascentral	rs80358155
openSNP	rs80358155
23andMe	rs80358155
SNPshot	rs80358155
SNPdbe	rs80358155
MSV3d	rs80358155
GWAS Ctlg	rs80358155

Max Magnitude

6

ClinVar
Risk	rs80358155(C;C)
Alt	rs80358155(C;C)
Reference	Rs80358155(A;A)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41251899T>G
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000112676.1,