|
rs572115942
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs953686324
|
|
TG |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1064794268
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
"MODY 2 presenting as neonatal hyperglycaemia: a need to reshape the definition of ""neonatal diabetes""?"
|
11079754 |
2000 |
|
rs1320702652
|
|
|
0.010 |
GeneticVariation |
BEFREE |
C34T AMPD1 polymorphism may be associated with reduced frequency of obesity in CAD patients and of hyperglycaemia and diabetes in both CAD and HF patients.
|
18855224 |
2009 |
|
rs1085307455
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria.
|
10753050 |
2000 |
|
rs1064793998
|
|
T |
0.720 |
CausalMutation |
CLINVAR |
A missense mutation, Val62Ala, in the glucokinase gene in a Norwegian family with maturity-onset diabetes of the young.
|
9736233 |
1998 |
|
rs59852838
|
|
|
0.010 |
GeneticVariation |
BEFREE |
A mutation in ABCC8/SUR1, leading to a Y356C substitution in the seventh membrane-spanning alpha-helix, was observed in a patient diagnosed with hyperglycemia at age 39 years and in two adult offspring with impaired insulin secretion.
|
18346985 |
2008 |
|
rs776793516
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
A rapid screening method for hepatocyte nuclear factor 1 alpha frameshift mutations; prevalence in maturity-onset diabetes of the young and late-onset non-insulin dependent diabetes.
|
9439666 |
1997 |
|
rs1045642
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ABCB1 rs1045642 was associated with risk of mucositis (P = 0.031), while PIK3R1 rs10515074 and RAPTOR rs9906827 were associated with hyperglycemia and non-infectious pneumonitis (P = 0.016 and 0.024, respectively).
|
28727815 |
2017 |
|
rs10515074
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ABCB1 rs1045642 was associated with risk of mucositis (P = 0.031), while PIK3R1 rs10515074 and RAPTOR rs9906827 were associated with hyperglycemia and non-infectious pneumonitis (P = 0.016 and 0.024, respectively).
|
28727815 |
2017 |
|
rs9906827
|
|
|
0.010 |
GeneticVariation |
BEFREE |
ABCB1 rs1045642 was associated with risk of mucositis (P = 0.031), while PIK3R1 rs10515074 and RAPTOR rs9906827 were associated with hyperglycemia and non-infectious pneumonitis (P = 0.016 and 0.024, respectively).
|
28727815 |
2017 |
|
rs1057524900
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents.
|
16602010 |
2006 |
|
rs1050828
|
|
|
0.010 |
GeneticVariation |
BEFREE |
After recalibration of the HbA<sub>1c</sub> level taking <i>HBB</i>-rs334 and <i>G6PD</i>-rs1050828 into account, the prevalence of hyperglycemia in carriers was similar to noncarriers (31.3% vs. 28.4%, <i>P</i> = 0.28).
|
31213470 |
2019 |
|
rs7903146
|
|
|
0.070 |
GeneticVariation |
BEFREE |
Also the well-known gene variants rs7903146 in TCF7L2, and rs17817449 in FTO, were nominally associated with hyperglycemia (rs7903146), as well as with higher fasting insulin levels (rs17817449).
|
30063936 |
2018 |
|
rs17817449
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Also the well-known gene variants rs7903146 in TCF7L2, and rs17817449 in FTO, were nominally associated with hyperglycemia (rs7903146), as well as with higher fasting insulin levels (rs17817449).
|
30063936 |
2018 |
|
rs1272388614
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Alternating hypoglycemia and hyperglycemia in a toddler with a homozygous p.R1419H ABCC8 mutation: an unusual clinical picture.
|
25720052 |
2015 |
|
rs1446306735
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Alternating hypoglycemia and hyperglycemia in a toddler with a homozygous p.R1419H ABCC8 mutation: an unusual clinical picture.
|
25720052 |
2015 |
|
rs7799039
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Among the candidate genes, only the <i>LEP</i> rs7799039 polymorphism demonstrated a significant association with hyperglycemia</span> (χ<sup>2</sup>=9.879, <i>P</i>=0.008) in patients treated with risperidone; patients with the AA genotype had the highest risk (41.1%), followed by those with AG (20.8%) and GG (0%) genotypes.
|
31496784 |
2019 |
|
rs1375557127
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Analysis of the HNF4 alpha gene in Caucasian type II diabetic nephropathic patients.
|
10768098 |
2000 |
|
rs137853238
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Anatomy of a homeoprotein revealed by the analysis of human MODY3 mutations.
|
10585442 |
1999 |
|
rs3856806
|
|
|
0.010 |
GeneticVariation |
BEFREE |
As ageing and increased body fat are the signs of insulin resistance, we have studied whether the presence of Pro12Ala and C1431T of peroxisome proliferator-activated receptor gamma 2 gene and Trp64Arg of beta 3-adrenergic receptor gene may predispose to the hyperglycaemia development in postmenopausal women, who have never undergone hypoglycaemic treatment.
|
29464546 |
2018 |
|
rs738409
|
|
|
0.010 |
GeneticVariation |
BEFREE |
At multivariate analysis, Fetuin-A levels were associated with BMI, triglycerides, hyperglycemia and PNPLA3 I148M (P = 0·034) independently also of age, sex and ALT levels.
|
24828988 |
2014 |
|
rs776793516
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors.
|
11272211 |
2001 |
|
rs193929375
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Both parents were heterozygous for R397L and had mild hyperglycemia.
|
15644838 |
2005 |
|
rs1392795567
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Cancer in chronic ulcerative colitis. Diagnostic role of segmental colonic lavage.
|
193395 |
1977 |