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rs80357410

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs80357410(C;C)
Make rs80357410(C;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position43124027
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs80357410
ebirs80357410
HLIrs80357410
Exacrs80357410
Varsomers80357410
Maprs80357410
PheGenIrs80357410
hapmaprs80357410
1000 genomesrs80357410
hgdprs80357410
ensemblrs80357410
gopubmedrs80357410
geneviewrs80357410
scholarrs80357410
googlers80357410
pharmgkbrs80357410
gwascentralrs80357410
openSNPrs80357410
23andMers80357410
23andMe allrs80357410
SNP Nexus

SNPshotrs80357410
SNPdbers80357410
MSV3drs80357410
GWAS Ctlgrs80357410
Max Magnitude0
ClinVar
Risk rs80357410(C;C)
Alt rs80357410(C;C)
Reference rs80357410(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.41276044A>G
CLNSRC ClinVar
CLNACC RCV000049104.2, RCV000111679.1,