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rs80357111

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357111(G;G)
Make rs80357111(G;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124095
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs80357111
ebirs80357111
HLIrs80357111
Exacrs80357111
Varsomers80357111
Maprs80357111
PheGenIrs80357111
hapmaprs80357111
1000 genomesrs80357111
hgdprs80357111
ensemblrs80357111
gopubmedrs80357111
geneviewrs80357111
scholarrs80357111
googlers80357111
pharmgkbrs80357111
gwascentralrs80357111
openSNPrs80357111
23andMers80357111
23andMe allrs80357111
SNP Nexus

SNPshotrs80357111
SNPdbers80357111
MSV3drs80357111
GWAS Ctlgrs80357111
Max Magnitude0
ClinVar
Risk rs80357111(C,G;C,G)
Alt rs80357111(C,G;C,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,