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rs7552722

From SNPedia

Orientationplus
Stabilizedplus
Make rs7552722(C;C)
Make rs7552722(C;T)
Make rs7552722(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position115378734
is asnp
is mentioned by
dbSNPrs7552722
dbSNP (classic)rs7552722
ClinGenrs7552722
ebirs7552722
HLIrs7552722
Exacrs7552722
Gnomadrs7552722
Varsomers7552722
LitVarrs7552722
Maprs7552722
PheGenIrs7552722
Biobankrs7552722
1000 genomesrs7552722
hgdprs7552722
ensemblrs7552722
geneviewrs7552722
scholarrs7552722
googlers7552722
pharmgkbrs7552722
gwascentralrs7552722
openSNPrs7552722
23andMers7552722
SNPshotrs7552722
SNPdbers7552722
MSV3drs7552722
GWAS Ctlgrs7552722
GMAF0.2709
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23535911]
Trait Non-alcoholic fatty liver disease
Title Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan.
Risk Allele A
P-val 7E-6
Odds Ratio 1.27 [1.00-1.61]