rs80358064

Orientation

minus

Stabilized

minus

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

Make rs80358064(C;C)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43115723

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs80358064
dbSNP (classic)	rs80358064
ClinGen	rs80358064
ebi	rs80358064
HLI	rs80358064
Exac	rs80358064
Gnomad	rs80358064
Varsome	rs80358064
LitVar	rs80358064
Map	rs80358064
PheGenI	rs80358064
Biobank	rs80358064
1000 genomes	rs80358064
hgdp	rs80358064
ensembl	rs80358064
geneview	rs80358064
scholar	rs80358064
google	rs80358064
pharmgkb	rs80358064
gwascentral	rs80358064
openSNP	rs80358064
23andMe	rs80358064
SNPshot	rs80358064
SNPdbe	rs80358064
MSV3d	rs80358064
GWAS Ctlg	rs80358064

Max Magnitude

6

ClinVar
Risk	rs80358064(C;C)
Alt	rs80358064(C;C)
Reference	Rs80358064(A;A)
Significance	Other
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41267740T>G
CLNSRC	Breast Cancer Information Core (BRCA1)
CLNACC	RCV000047430.2, RCV000111851.1,