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rs4849121

From SNPedia

Orientationplus
Stabilizedplus
Make rs4849121(A;A)
Make rs4849121(A;G)
Make rs4849121(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position110842129
GeneACOXL
is asnp
is mentioned by
dbSNPrs4849121
dbSNP (classic)rs4849121
ClinGenrs4849121
ebirs4849121
HLIrs4849121
Exacrs4849121
Gnomadrs4849121
Varsomers4849121
LitVarrs4849121
Maprs4849121
PheGenIrs4849121
Biobankrs4849121
1000 genomesrs4849121
hgdprs4849121
ensemblrs4849121
geneviewrs4849121
scholarrs4849121
googlers4849121
pharmgkbrs4849121
gwascentralrs4849121
openSNPrs4849121
23andMers4849121
SNPshotrs4849121
SNPdbers4849121
MSV3drs4849121
GWAS Ctlgrs4849121
GMAF0.4747
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 22197929]
Trait
Title A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy.
Risk Allele G
P-val 4E-7
Odds Ratio 1.1500 None