Have questions? Visit https://www.reddit.com/r/SNPedia

rs4859146

From SNPedia

Orientationplus
Stabilizedplus
Make rs4859146(C;C)
Make rs4859146(C;T)
Make rs4859146(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position182963952
GeneDCUN1D1
is asnp
is mentioned by
dbSNPrs4859146
ebirs4859146
HLIrs4859146
Exacrs4859146
Varsomers4859146
Maprs4859146
PheGenIrs4859146
hapmaprs4859146
1000 genomesrs4859146
hgdprs4859146
ensemblrs4859146
gopubmedrs4859146
geneviewrs4859146
scholarrs4859146
googlers4859146
pharmgkbrs4859146
gwascentralrs4859146
openSNPrs4859146
23andMers4859146
23andMe allrs4859146
SNP Nexus

SNPshotrs4859146
SNPdbers4859146
MSV3drs4859146
GWAS Ctlgrs4859146
GMAF0.4118
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19473369] DCUN1D1 is a risk factor for frontotemporal lobar degeneration