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

rs4902647

From SNPedia

Orientationplus
Stabilizedplus
Make rs4902647(C;C)
Make rs4902647(C;T)
Make rs4902647(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position68787474
GeneZFP36L1
is asnp
is mentioned by
dbSNPrs4902647
ebirs4902647
HLIrs4902647
Exacrs4902647
Varsomers4902647
Maprs4902647
PheGenIrs4902647
hapmaprs4902647
1000 genomesrs4902647
hgdprs4902647
ensemblrs4902647
gopubmedrs4902647
geneviewrs4902647
scholarrs4902647
googlers4902647
pharmgkbrs4902647
gwascentralrs4902647
openSNPrs4902647
23andMers4902647
23andMe allrs4902647
SNP Nexus

SNPshotrs4902647
SNPdbers4902647
MSV3drs4902647
GWAS Ctlgrs4902647
GMAF0.4972
Max Magnitude
? (C;C) (C;T) (T;T) 28
23andMe blog multiple sclerosis rs4902647 ZFP36L1 T 0.88
GWAS snp
PMID [PMID 21833088OA-icon.png]
Trait
Title Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Risk Allele G
P-val 9E-12
Odds Ratio 1.1100 [1.10-1.13]