Rs1169310

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Orientationplus
Make rs1169310(A;A)
Make rs1169310(A;G)
Make rs1169310(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position121001630
GeneHNF1A
is asnp
is mentioned by
dbSNPrs1169310
PheGenIrs1169310
nextbiors1169310
hapmaprs1169310
1000 genomesrs1169310
hgdprs1169310
ensemblrs1169310
gopubmedrs1169310
geneviewrs1169310
scholarrs1169310
googlers1169310
pharmgkbrs1169310
gwascentralrs1169310
openSNPrs1169310
23andMers1169310
23andMe allrs1169310
SNP Nexus

SNPshotrs1169310
SNPdbers1169310
MSV3drs1169310
GMAF0.3669
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS
SNP rs1169310
PubMedID [PMID 18439552OA-icon.png]
Condition C-reactive protein
Gene HNF1A
Risk Allele A
pValue 2.00E-008
OR 0.13
95% CI 0.08-0.17) mg/l decrease in log(CRP) leve




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


[PMID 21195701] Effect of obesity on the association between common variations in the HNF1A gene region and C-reactive protein level in Taiwanese.


GET Evidence
rs1169310
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.320312
summary