rs80358051

Orientation

minus

Stabilized

minus

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

Make rs80358051(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43104264

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs80358051
dbSNP (classic)	rs80358051
ClinGen	rs80358051
ebi	rs80358051
HLI	rs80358051
Exac	rs80358051
Gnomad	rs80358051
Varsome	rs80358051
LitVar	rs80358051
Map	rs80358051
PheGenI	rs80358051
Biobank	rs80358051
1000 genomes	rs80358051
hgdp	rs80358051
ensembl	rs80358051
geneview	rs80358051
scholar	rs80358051
google	rs80358051
pharmgkb	rs80358051
gwascentral	rs80358051
openSNP	rs80358051
23andMe	rs80358051
SNPshot	rs80358051
SNPdbe	rs80358051
MSV3d	rs80358051
GWAS Ctlg	rs80358051

Max Magnitude

6

ClinVar
Risk	rs80358051(G;G)
Alt	rs80358051(G;G)
Reference	Rs80358051(C;C)
Significance	Other
Disease	Breast-ovarian cancer Familial cancer of breast Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA1
CLNDBN	Breast-ovarian cancer, familial 1 Familial cancer of breast Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000017.10:g.41256281G>C
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000031082.5, RCV000048048.2, RCV000219090.1,