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rs11083271

From SNPedia

Orientationplus
Stabilizedplus
Make rs11083271(C;C)
Make rs11083271(C;T)
Make rs11083271(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position28346095
is asnp
is mentioned by
dbSNPrs11083271
dbSNP (classic)rs11083271
ClinGenrs11083271
ebirs11083271
HLIrs11083271
Exacrs11083271
Gnomadrs11083271
Varsomers11083271
LitVarrs11083271
Maprs11083271
PheGenIrs11083271
Biobankrs11083271
1000 genomesrs11083271
hgdprs11083271
ensemblrs11083271
geneviewrs11083271
scholarrs11083271
googlers11083271
pharmgkbrs11083271
gwascentralrs11083271
openSNPrs11083271
23andMers11083271
SNPshotrs11083271
SNPdbers11083271
MSV3drs11083271
GWAS Ctlgrs11083271
GMAF0.3095
Max Magnitude0
? (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 A
P-val 0.000008
Odds Ratio 0.61 [NR] unit increase