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rs4237591

From SNPedia

Orientationplus
Stabilizedplus
Make rs4237591(C;C)
Make rs4237591(C;T)
Make rs4237591(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position98595538
is asnp
is mentioned by
dbSNPrs4237591
ebirs4237591
HLIrs4237591
Exacrs4237591
Varsomers4237591
Maprs4237591
PheGenIrs4237591
hapmaprs4237591
1000 genomesrs4237591
hgdprs4237591
ensemblrs4237591
gopubmedrs4237591
geneviewrs4237591
scholarrs4237591
googlers4237591
pharmgkbrs4237591
gwascentralrs4237591
openSNPrs4237591
23andMers4237591
23andMe allrs4237591
SNP Nexus

SNPshotrs4237591
SNPdbers4237591
MSV3drs4237591
GWAS Ctlgrs4237591
GMAF0.4123
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20708005OA-icon.png]
Trait
Title Genome-Wide Association Study Identifies Variants Associated with Histologic Features of Nonalcoholic Fatty Liver Disease
Risk Allele G
P-val 0.000002
Odds Ratio 0.33 [NR] unit decrease