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: 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: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C2711227
Disease:
Steatohepatitis
0.010 GeneticVariation BEFREE In addition, CMA suggested that rs13266634 protects against POHG directly and indirectly through its influence on liver steatosis and central adiposity. 31220282 2019
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0032460
Disease:
Polycystic Ovary Syndrome
0.010 GeneticVariation BEFREE No statistically significant differences in genotype and allele frequencies of single nucleotide polymorphism (SNP) rs13266634</span> in gene SLC30A8 were found between patients with polycystic ovary syndrome (PCOS) and healthy controls. 19108828 2009
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0028754
Disease:
Obesity
0.030 GeneticVariation BEFREE In the present study, we examined the association between variants in fat mass- and obesity-associated [rs9939609 (A/T)], melanocortin 4 receptor [rs17782313 (C/T), and rs12970134 (A/G)], SLC30A8 [rs13266634 (C/T)], and a member of the potassium voltage-gated channels [rs2237892(C/T)] genes in diabetes patients from Saudi Arabia. 25501231 2014
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0028754
Disease:
Obesity
0.030 GeneticVariation BEFREE An interaction was also observed between rs13266634 and salty snacks at the risk of abdominal obesity (P interaction < 0.05). 28490771 2017
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0028754
Disease:
Obesity
0.030 GeneticVariation BEFREE Most notably, 5 SNPs from 5 genes [body mass index (BMI), hip circumference: rs3751812/FTO; fasting plasma glucose, hemoglobin A1c: rs4607517/GCK; very-low-density lipoprotein: rs10830963/MTNR1B; BMI: rs13266634/SLC30A8, and total cholesterol, low-density lipoprotein: rs7578597/THADA] were significantly associated with obesity, glycemic, and lipid phenotypes when using the multiple testing significance threshold of 0.0015. 25060389 2014
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0524620
Disease:
Metabolic Syndrome X
0.010 GeneticVariation BEFREE An interaction was observed between rs13266634 and the omega-3 fatty acid intakes on the risk of M</span>etS in subjects with the CC genotype (P interaction < 0.01). 28490771 2017
dbSNP: rs4876369
rs4876369
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Diabetes status modified the associations between rs4876369 and rs2241745 and BC incidence, on the multiplicative interaction scale. 30457165 2019
dbSNP: rs1155178
rs1155178
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11781136
rs11781136
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
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: rs13253360
rs13253360
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs13266865
rs13266865
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 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: rs17812503
rs17812503
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute
C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
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: rs6997279
rs6997279
Entrez Id: 169026
Gene Symbol: SLC30A8
SLC30A8
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.700 GeneticVariation GWASCAT A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. 29703844 2018
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: rs11558471
rs11558471
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0202098
Disease:
Insulin measurement
A 0.800 GeneticVariation GWASCAT Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. 21873549 2011
dbSNP: rs11558471
rs11558471
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0202098
Disease:
Insulin measurement
A 0.800 GeneticVariation GWASDB Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. 21873549 2011
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0271650
Disease:
Impaired glucose tolerance
0.010 GeneticVariation BEFREE And the pooled odds ratio (OR) for allelic frequency comparison showed that rs13266634 C/T polymorphism was also significantly associated with IGT: OR=1.15, 95% CI=1.06-1.26, P<0.001, P(heterogeneity)=0.364. 21131091 2011
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0020459
Disease:
Hyperinsulinism
0.010 GeneticVariation BEFREE Consistent with these findings, ZnT8KO mice and human individuals carrying rs13266634, a major risk allele of SLC30A8, exhibited increased insulin clearance, as assessed by c-peptide/insulin ratio. 24051378 2013
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0020456
Disease:
Hyperglycemia
0.010 GeneticVariation BEFREE The Role of Genetic Variant rs13266634 in SLC30A8/ZnT8 in Post-Operative Hyperglycemia after Major Abdominal Surgery. 31220282 2019
dbSNP: rs13266634
rs13266634
Entrez Id: 169026;105375716
Gene Symbol: SLC30A8;LOC105375716
SLC30A8;LOC105375716
CUI: C0019196
Disease:
Hepatitis C
0.010 GeneticVariation BEFREE SLC30A8 rs13266634 polymorphism is related to a favorable cardiometabolic lipid profile in HIV/hepatitis C virus-coinfected patients. 24499956 2014