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rs9977253

From SNPedia

Orientationplus
Stabilizedplus
Make rs9977253(C;C)
Make rs9977253(C;T)
Make rs9977253(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position25272769
is asnp
is mentioned by
dbSNPrs9977253
ebirs9977253
HLIrs9977253
Exacrs9977253
Varsomers9977253
Maprs9977253
PheGenIrs9977253
hapmaprs9977253
1000 genomesrs9977253
hgdprs9977253
ensemblrs9977253
gopubmedrs9977253
geneviewrs9977253
scholarrs9977253
googlers9977253
pharmgkbrs9977253
gwascentralrs9977253
openSNPrs9977253
23andMers9977253
23andMe allrs9977253
SNP Nexus

SNPshotrs9977253
SNPdbers9977253
MSV3drs9977253
GWAS Ctlgrs9977253
GMAF0.1671
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 0.000005
Odds Ratio 0.76 [NR] unit increase