rs80357111

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs80357111(G;G)

Make rs80357111(G;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43124095

Gene	BRCA1, NBR2

is a	snp
is	mentioned by
dbSNP	rs80357111
dbSNP (classic)	rs80357111
ClinGen	rs80357111
ebi	rs80357111
HLI	rs80357111
Exac	rs80357111
Gnomad	rs80357111
Varsome	rs80357111
LitVar	rs80357111
Map	rs80357111
PheGenI	rs80357111
Biobank	rs80357111
1000 genomes	rs80357111
hgdp	rs80357111
ensembl	rs80357111
geneview	rs80357111
scholar	rs80357111
google	rs80357111
pharmgkb	rs80357111
gwascentral	rs80357111
openSNP	rs80357111
23andMe	rs80357111
SNPshot	rs80357111
SNPdbe	rs80357111
MSV3d	rs80357111
GWAS Ctlg	rs80357111

Max Magnitude

0

ClinVar
Risk	rs80357111(C;C) rs80357111(G;G)
Alt	rs80357111(C;C) rs80357111(G;G)
Reference	Rs80357111(T;T)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	NBR2 BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41276112A>C; NC_000017.10:g.41276112A>G
CLNSRC	ClinVar
CLNACC	RCV000048038.2, RCV000111546.1, RCV000048037.2, RCV000111545.1,