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rs2986971

From SNPedia

Orientationplus
Stabilizedplus
Make rs2986971(A;A)
Make rs2986971(A;G)
Make rs2986971(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position29807699
is asnp
is mentioned by
dbSNPrs2986971
ebirs2986971
HLIrs2986971
Exacrs2986971
Varsomers2986971
Maprs2986971
PheGenIrs2986971
hapmaprs2986971
1000 genomesrs2986971
hgdprs2986971
ensemblrs2986971
gopubmedrs2986971
geneviewrs2986971
scholarrs2986971
googlers2986971
pharmgkbrs2986971
gwascentralrs2986971
openSNPrs2986971
23andMers2986971
23andMe allrs2986971
SNP Nexus

SNPshotrs2986971
SNPdbers2986971
MSV3drs2986971
GWAS Ctlgrs2986971
GMAF0.494
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 G
P-val 0.000003
Odds Ratio 0.49 [NR] unit increase