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rs80357316

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357316(C;C)
Make rs80357316(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124053
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs80357316
ebirs80357316
HLIrs80357316
Exacrs80357316
Varsomers80357316
Maprs80357316
PheGenIrs80357316
hapmaprs80357316
1000 genomesrs80357316
hgdprs80357316
ensemblrs80357316
gopubmedrs80357316
geneviewrs80357316
scholarrs80357316
googlers80357316
pharmgkbrs80357316
gwascentralrs80357316
openSNPrs80357316
23andMers80357316
23andMe allrs80357316
SNP Nexus

SNPshotrs80357316
SNPdbers80357316
MSV3drs80357316
GWAS Ctlgrs80357316
Max Magnitude0
ClinVar
Risk rs80357316(C;C)
Alt rs80357316(C;C)
Reference rs80357316(T;T)
Significance Untested
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.41276070A>G
CLNSRC ClinVar
CLNACC RCV000048581.2, RCV000111641.2,