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rs879255496

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879255496(A;A)
Make rs879255496(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position43124020
GeneBRCA1, NBR2
is asnp
is mentioned by
dbSNPrs879255496
ebirs879255496
HLIrs879255496
Exacrs879255496
Varsomers879255496
Maprs879255496
PheGenIrs879255496
hapmaprs879255496
1000 genomesrs879255496
hgdprs879255496
ensemblrs879255496
gopubmedrs879255496
geneviewrs879255496
scholarrs879255496
googlers879255496
pharmgkbrs879255496
gwascentralrs879255496
openSNPrs879255496
23andMers879255496
23andMe allrs879255496
SNP Nexus

SNPshotrs879255496
SNPdbers879255496
MSV3drs879255496
GWAS Ctlgrs879255496
Max Magnitude0
ClinVar
Risk rs879255496(A;A)
Alt rs879255496(A;A)
Reference rs879255496(T;T)
Significance Pathogenic
Disease Breast-ovarian cancer
Variation info
Gene NBR2 BRCA1
CLNDBN Breast-ovarian cancer, familial 1
Reversed 1
HGVS NC_000017.10:g.41276037A>T
CLNSRC
CLNACC RCV000239011.1,