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rs1169310

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1169310(A;A)
Make rs1169310(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position121001630
GeneHNF1A
is asnp
is mentioned by
dbSNPrs1169310
dbSNP (classic)rs1169310
ClinGenrs1169310
ebirs1169310
HLIrs1169310
Exacrs1169310
Gnomadrs1169310
Varsomers1169310
LitVarrs1169310
Maprs1169310
PheGenIrs1169310
Biobankrs1169310
1000 genomesrs1169310
hgdprs1169310
ensemblrs1169310
geneviewrs1169310
scholarrs1169310
googlers1169310
pharmgkbrs1169310
gwascentralrs1169310
openSNPrs1169310
23andMers1169310
SNPshotrs1169310
SNPdbers1169310
MSV3drs1169310
GWAS Ctlgrs1169310
GMAF0.3669
Max Magnitude0
? (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.



ClinVar
Risk rs1169310(A;A)
Alt rs1169310(A;A)
Reference Rs1169310(G;G)
Significance Non-pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene HNF1A
CLNDBN Maturity-onset diabetes of the young
Reversed 0
HGVS NC_000012.11:g.121439433G>A
CLNSRC
CLNACC RCV000402135.1,