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rs2710833

From SNPedia

Orientationplus
Stabilizedplus
Make rs2710833(C;C)
Make rs2710833(C;T)
Make rs2710833(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position168488807
is asnp
is mentioned by
dbSNPrs2710833
ebirs2710833
HLIrs2710833
Exacrs2710833
Varsomers2710833
Maprs2710833
PheGenIrs2710833
hapmaprs2710833
1000 genomesrs2710833
hgdprs2710833
ensemblrs2710833
gopubmedrs2710833
geneviewrs2710833
scholarrs2710833
googlers2710833
pharmgkbrs2710833
gwascentralrs2710833
openSNPrs2710833
23andMers2710833
23andMe allrs2710833
SNP Nexus

SNPshotrs2710833
SNPdbers2710833
MSV3drs2710833
GWAS Ctlgrs2710833
GMAF0.1529
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 6E-7
Odds Ratio 0.41 [NR] unit increase