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rs4909764

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common genotype
Make rs4909764(C;C)
Make rs4909764(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position138243675
GeneFAM135B
is asnp
is mentioned by
dbSNPrs4909764
dbSNP (classic)rs4909764
ClinGenrs4909764
ebirs4909764
HLIrs4909764
Exacrs4909764
Gnomadrs4909764
Varsomers4909764
LitVarrs4909764
Maprs4909764
PheGenIrs4909764
Biobankrs4909764
1000 genomesrs4909764
hgdprs4909764
ensemblrs4909764
geneviewrs4909764
scholarrs4909764
googlers4909764
pharmgkbrs4909764
gwascentralrs4909764
openSNPrs4909764
23andMers4909764
SNPshotrs4909764
SNPdbers4909764
MSV3drs4909764
GWAS Ctlgrs4909764
GMAF0.07025
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 22228203OA-icon.png]
Trait
Title A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.
Risk Allele
P-val 0.000002
Odds Ratio None None