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rs1390096

From SNPedia

Orientationplus
Stabilizedplus
Make rs1390096(A;A)
Make rs1390096(A;G)
Make rs1390096(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position11501980
is asnp
is mentioned by
dbSNPrs1390096
ebirs1390096
HLIrs1390096
Exacrs1390096
Varsomers1390096
Maprs1390096
PheGenIrs1390096
hapmaprs1390096
1000 genomesrs1390096
hgdprs1390096
ensemblrs1390096
gopubmedrs1390096
geneviewrs1390096
scholarrs1390096
googlers1390096
pharmgkbrs1390096
gwascentralrs1390096
openSNPrs1390096
23andMers1390096
23andMe allrs1390096
SNP Nexus

SNPshotrs1390096
SNPdbers1390096
MSV3drs1390096
GWAS Ctlgrs1390096
GMAF0.2677
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 22719876OA-icon.png]
Trait
Title Genetic Polymorphisms of the Human PNPLA3 Gene Are Strongly Associated with Severity of Non-Alcoholic Fatty Liver Disease in Japanese.
Risk Allele A
P-val 0.000003
Odds Ratio 1.4400 None