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rs6691847

From SNPedia

Orientationplus
Stabilizedplus
Make rs6691847(C;C)
Make rs6691847(C;T)
Make rs6691847(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position29792805
is asnp
is mentioned by
dbSNPrs6691847
ebirs6691847
HLIrs6691847
Exacrs6691847
Varsomers6691847
Maprs6691847
PheGenIrs6691847
hapmaprs6691847
1000 genomesrs6691847
hgdprs6691847
ensemblrs6691847
gopubmedrs6691847
geneviewrs6691847
scholarrs6691847
googlers6691847
pharmgkbrs6691847
gwascentralrs6691847
openSNPrs6691847
23andMers6691847
23andMe allrs6691847
SNP Nexus

SNPshotrs6691847
SNPdbers6691847
MSV3drs6691847
GWAS Ctlgrs6691847
GMAF0.1818
Max Magnitude
? (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 C
P-val 7E-6
Odds Ratio 1.32 [0.98-1.77]