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rs2358462

From SNPedia

Orientationplus
Stabilizedplus
Make rs2358462(C;C)
Make rs2358462(C;T)
Make rs2358462(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position148649528
is asnp
is mentioned by
dbSNPrs2358462
ebirs2358462
HLIrs2358462
Exacrs2358462
Varsomers2358462
Maprs2358462
PheGenIrs2358462
hapmaprs2358462
1000 genomesrs2358462
hgdprs2358462
ensemblrs2358462
gopubmedrs2358462
geneviewrs2358462
scholarrs2358462
googlers2358462
pharmgkbrs2358462
gwascentralrs2358462
openSNPrs2358462
23andMers2358462
23andMe allrs2358462
SNP Nexus

SNPshotrs2358462
SNPdbers2358462
MSV3drs2358462
GWAS Ctlgrs2358462
GMAF0.3104
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 G
P-val 0.000004
Odds Ratio 0.60 [NR] unit increase