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rs10067427

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0
Make rs10067427(A;G)
Make rs10067427(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position100006343
is asnp
is mentioned by
dbSNPrs10067427
ebirs10067427
HLIrs10067427
Exacrs10067427
Varsomers10067427
Maprs10067427
PheGenIrs10067427
hapmaprs10067427
1000 genomesrs10067427
hgdprs10067427
ensemblrs10067427
gopubmedrs10067427
geneviewrs10067427
scholarrs10067427
googlers10067427
pharmgkbrs10067427
gwascentralrs10067427
openSNPrs10067427
23andMers10067427
23andMe allrs10067427
SNP Nexus

SNPshotrs10067427
SNPdbers10067427
MSV3drs10067427
GWAS Ctlgrs10067427
GMAF0.4206
Max Magnitude0
? (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 0.000005
Odds Ratio 0.75 [NR] unit increase