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rs1529093

From SNPedia

Orientationplus
Stabilizedplus
Make rs1529093(C;C)
Make rs1529093(C;T)
Make rs1529093(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position177044867
is asnp
is mentioned by
dbSNPrs1529093
ebirs1529093
HLIrs1529093
Exacrs1529093
Varsomers1529093
Maprs1529093
PheGenIrs1529093
hapmaprs1529093
1000 genomesrs1529093
hgdprs1529093
ensemblrs1529093
gopubmedrs1529093
geneviewrs1529093
scholarrs1529093
googlers1529093
pharmgkbrs1529093
gwascentralrs1529093
openSNPrs1529093
23andMers1529093
23andMe allrs1529093
SNP Nexus

SNPshotrs1529093
SNPdbers1529093
MSV3drs1529093
GWAS Ctlgrs1529093
GMAF0.4559
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 A
P-val 0.000002
Odds Ratio 4.13 [NR] unit increase