Rs10885122

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ReferenceGRCh37 37.1/131
Chromosome10
Position113042093
is asnp
is mentioned by
dbSNPrs10885122
Exacrs10885122
PheGenIrs10885122
nextbiors10885122
hapmaprs10885122
1000 genomesrs10885122
hgdprs10885122
ensemblrs10885122
gopubmedrs10885122
geneviewrs10885122
scholarrs10885122
googlers10885122
pharmgkbrs10885122
gwascentralrs10885122
openSNPrs10885122
23andMers10885122
23andMe allrs10885122
SNP Nexus

SNPshotrs10885122
SNPdbers10885122
MSV3drs10885122
GMAF0.2649
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 20081858OA-icon.png]
Trait Fasting glucose-related traits
Title New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Risk Allele G
P-val 0.000002
Odds Ratio None None



[PMID 21887289OA-icon.png] Glucose-Raising Genetic Variants in MADD and ADCY5 Impair Conversion of Proinsulin to Insulin


[PMID 20870969OA-icon.png] Genetic predisposition to long-term nondiabetic deteriorations in glucose homeostasis: Ten-year follow-up of the GLACIER study.


[PMID 21455730OA-icon.png] Variants of ADRA2A are associated with fasting glucose, blood pressure, body mass index and type 2 diabetes risk: meta-analysis of four prospective studies.

GWAS snp
PMID [PMID 22581228OA-icon.png]
Trait
Title A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
Risk Allele
P-val 9E-8
Odds Ratio None None


GET Evidence
rs10885122
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.617188
summary



[PMID 22698489] Nonfasting glucose, ischemic heart disease, and myocardial infarction: a Mendelian randomization study.


[PMID 23466530] SCN1AIVS5-91G>A polymorphism is associated with susceptibility to epilepsy but not with drug responsiveness.