SLC30A8, solute carrier family 30 member 8, 169026

N. diseases: 63; N. variants: 23
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		T 1.000 SusceptibilityMutation CLINVAR
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		T 1.000 GeneticVariation GWASCAT Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590 2017
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0428568
Disease:
Fasting blood glucose measurement 		T 0.700 GeneticVariation GWASCAT Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. 25625282 2015
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0428568
Disease:
Fasting blood glucose measurement 		T 0.700 GeneticVariation GWASCAT Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. 28270201 2017
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0202236
Disease:
Triglycerides measurement 		T 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs6987643
rs6987643
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.820 GeneticVariation GWASDB Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. 22693455 2012
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.820 GeneticVariation GWASCAT Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. 31118516 2019
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.820 GeneticVariation GWASCAT Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922 2012
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.820 GeneticVariation GWASDB Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. 20581827 2010
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.820 GeneticVariation GWASCAT Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. 24509480 2014
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.820 GeneticVariation GWASCAT Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. 20581827 2010
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.820 GeneticVariation GWASCAT Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively. 26961502 2016
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.820 GeneticVariation GWASDB Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. 24509480 2014
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.820 GeneticVariation GWASCAT Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. 22693455 2012
dbSNP: rs11558471
rs11558471
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0428568
Disease:
Fasting blood glucose measurement 		G 0.800 GeneticVariation GWASCAT Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. 25631608 2015
dbSNP: rs11558471
rs11558471
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0428568
Disease:
Fasting blood glucose measurement 		G 0.800 GeneticVariation GWASCAT Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. 28270201 2017
dbSNP: rs11558471
rs11558471
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0202098
Disease:
Insulin measurement 		G 0.800 GeneticVariation GWASCAT Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. 23263489 2013
dbSNP: rs3019885
rs3019885
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0004096
Disease:
Asthma 		G 0.800 GeneticVariation GWASCAT Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations. 21814517 2011
dbSNP: rs3019885
rs3019885
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0004096
Disease:
Asthma 		G 0.800 GeneticVariation GWASDB Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations. 21814517 2011
dbSNP: rs11989343
rs11989343
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17744945
rs17744945
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17745016
rs17745016
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs3802177
rs3802177
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C1305855
Disease:
Body mass index 		G 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. 28892062 2017
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		C 1.000 GeneticVariation GWASCAT A genome-wide association study identifies novel risk loci for type 2 diabetes. 17293876 2007