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rs4846922

From SNPedia

Orientationplus
Stabilizedplus
Make rs4846922(C;C)
Make rs4846922(C;T)
Make rs4846922(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position230171436
GeneGALNT2
is asnp
is mentioned by
dbSNPrs4846922
ebirs4846922
HLIrs4846922
Exacrs4846922
Varsomers4846922
Maprs4846922
PheGenIrs4846922
hapmaprs4846922
1000 genomesrs4846922
hgdprs4846922
ensemblrs4846922
gopubmedrs4846922
geneviewrs4846922
scholarrs4846922
googlers4846922
pharmgkbrs4846922
gwascentralrs4846922
openSNPrs4846922
23andMers4846922
23andMe allrs4846922
SNP Nexus

SNPshotrs4846922
SNPdbers4846922
MSV3drs4846922
GWAS Ctlgrs4846922
GMAF0.3581
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22399527OA-icon.png]
Trait
Title Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.
Risk Allele T
P-val 4E-8
Odds Ratio 0.0800 None