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rs878855123

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855123(G;T)
Make rs878855123(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position23641151
GeneDCTN5, PALB2
is asnp
is mentioned by
dbSNPrs878855123
ebirs878855123
HLIrs878855123
Exacrs878855123
Varsomers878855123
Maprs878855123
PheGenIrs878855123
hapmaprs878855123
1000 genomesrs878855123
hgdprs878855123
ensemblrs878855123
gopubmedrs878855123
geneviewrs878855123
scholarrs878855123
googlers878855123
pharmgkbrs878855123
gwascentralrs878855123
openSNPrs878855123
23andMers878855123
23andMe allrs878855123
SNP Nexus

SNPshotrs878855123
SNPdbers878855123
MSV3drs878855123
GWAS Ctlgrs878855123
Max Magnitude0
ClinVar
Risk rs878855123(T;T)
Alt rs878855123(T;T)
Reference rs878855123(G;G)
Significance Pathogenic
Disease Familial cancer of breast
Variation info
Gene PALB2 DCTN5
CLNDBN Familial cancer of breast
Reversed 1
HGVS NC_000016.9:g.23652472C>A
CLNSRC
CLNACC RCV000231797.1,