Have questions? Visit https://www.reddit.com/r/SNPedia

rs1169313

From SNPedia

Orientationplus
Stabilizedplus
Make rs1169313(C;C)
Make rs1169313(C;T)
Make rs1169313(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position121004867
GeneC12orf43
is asnp
is mentioned by
dbSNPrs1169313
ebirs1169313
HLIrs1169313
Exacrs1169313
Varsomers1169313
Maprs1169313
PheGenIrs1169313
hapmaprs1169313
1000 genomesrs1169313
hgdprs1169313
ensemblrs1169313
gopubmedrs1169313
geneviewrs1169313
scholarrs1169313
googlers1169313
pharmgkbrs1169313
gwascentralrs1169313
openSNPrs1169313
23andMers1169313
23andMe allrs1169313
SNP Nexus

SNPshotrs1169313
SNPdbers1169313
MSV3drs1169313
GWAS Ctlgrs1169313
GMAF0.3682
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18940312OA-icon.png]
Trait Plasma levels of liver enzymes
Title Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes
Risk Allele C
P-val 2E-10
Odds Ratio 0.01 [0.003-0.007] U/L decrease
OMIM612366
DescGAMMA GLUTAMYLTRANSFERASE, PLASMA LEVEL OF, QUANTITATIVE TRAIT LOCUS
Variant
Relatedalso
[PMID 18439552OA-icon.png] Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.


[PMID 19198612OA-icon.png] New susceptibility locus for coronary artery disease on chromosome 3q22.3.


[PMID 19474294OA-icon.png] Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.


GET Evidence
rs1169313
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.320312
summary