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rs2049953

From SNPedia

Orientationplus
Stabilizedplus
Make rs2049953(A;A)
Make rs2049953(A;C)
Make rs2049953(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position134817852
is asnp
is mentioned by
dbSNPrs2049953
ebirs2049953
HLIrs2049953
Exacrs2049953
Varsomers2049953
Maprs2049953
PheGenIrs2049953
hapmaprs2049953
1000 genomesrs2049953
hgdprs2049953
ensemblrs2049953
gopubmedrs2049953
geneviewrs2049953
scholarrs2049953
googlers2049953
pharmgkbrs2049953
gwascentralrs2049953
openSNPrs2049953
23andMers2049953
23andMe allrs2049953
SNP Nexus

SNPshotrs2049953
SNPdbers2049953
MSV3drs2049953
GWAS Ctlgrs2049953
GMAF0.2039
Max Magnitude
? (A;A) (A;C) (C;C) 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 C
P-val 0.000004
Odds Ratio 0.26 [NR] unit increase