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rs11669592

From SNPedia

Orientationplus
Stabilizedplus
Make rs11669592(A;A)
Make rs11669592(A;G)
Make rs11669592(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position3318512
is asnp
is mentioned by
dbSNPrs11669592
ebirs11669592
HLIrs11669592
Exacrs11669592
Varsomers11669592
Maprs11669592
PheGenIrs11669592
hapmaprs11669592
1000 genomesrs11669592
hgdprs11669592
ensemblrs11669592
gopubmedrs11669592
geneviewrs11669592
scholarrs11669592
googlers11669592
pharmgkbrs11669592
gwascentralrs11669592
openSNPrs11669592
23andMers11669592
23andMe allrs11669592
SNP Nexus

SNPshotrs11669592
SNPdbers11669592
MSV3drs11669592
GWAS Ctlgrs11669592
GMAF0.4444
Max Magnitude
? (A;A) (A;G) (G;G) 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 A
P-val 0.000004
Odds Ratio 1.31 [NR] unit decrease