PDE10A, phosphodiesterase 10A, 10846

N. diseases: 97; N. variants: 26
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2983533
rs2983533
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3002433
rs3002433
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3008034
rs3008034
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0202230
Disease:
Thyroid stimulating hormone measurement
C 0.700 GeneticVariation GWASCAT Whole-genome sequence-based analysis of thyroid function. 25743335 2015
dbSNP: rs3008034
rs3008034
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0202230
Disease:
Thyroid stimulating hormone measurement
0.700 GeneticVariation GWASCAT A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents. 28333968 2017
dbSNP: rs4305701
rs4305701
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6914479
rs6914479
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0014772
Disease:
Red Blood Cell Count measurement
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6932812
rs6932812
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs753760
rs753760
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0441683
Disease:
Hormone measurement
C 0.700 GeneticVariation GWASCAT A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function. 23408906 2013
dbSNP: rs7744143
rs7744143
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0428883
Disease:
Diastolic blood pressure
A 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs7744143
rs7744143
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0001948
Disease:
Alcohol consumption
A 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs778899140
rs778899140
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C1858120
Disease:
Generalized hypotonia
C 0.700 GeneticVariation CLINVAR
dbSNP: rs778899140
rs778899140
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0557874
Disease:
Global developmental delay
C 0.700 GeneticVariation CLINVAR
dbSNP: rs903432
rs903432
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0428883
Disease:
Diastolic blood pressure
A 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs903432
rs903432
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0871470
Disease:
Systolic Pressure
A 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs9457107
rs9457107
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0005612
Disease:
Birth Weight
C 0.700 GeneticVariation GWASCAT Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. 31043758 2019
dbSNP: rs1039002
rs1039002
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic
0.010 GeneticVariation BEFREE Bipolar disorder with psychosis and/or substance abuse in the absence of alcohol dependence was associated with the rare variant rs1039002 in the vicinity of the gene phosphodiesterase 10A (PDE10A) on chromosome 6q27 (p = 1.7×10⁻⁸). 22205951 2011
dbSNP: rs1039002
rs1039002
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0740858
Disease:
Substance abuse problem
0.010 GeneticVariation BEFREE Bipolar disorder with psychosis and/or substance abuse in the absence of alcohol dependence was associated with the rare variant rs1039002 in the vicinity of the gene phosphodiesterase 10A (PDE10A) on chromosome 6q27 (p = 1.7×10⁻⁸). 22205951 2011
dbSNP: rs1039002
rs1039002
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0349204
Disease:
Nonorganic psychosis
0.010 GeneticVariation BEFREE Bipolar disorder with psychosis and/or substance abuse in the absence of alcohol dependence was associated with the rare variant rs1039002 in the vicinity of the gene phosphodiesterase 10A (PDE10A) on chromosome 6q27 (p = 1.7×10⁻⁸). 22205951 2011
dbSNP: rs1039002
rs1039002
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0033975
Disease:
Psychotic Disorders
0.010 GeneticVariation BEFREE Bipolar disorder with psychosis and/or substance abuse in the absence of alcohol dependence was associated with the rare variant rs1039002 in the vicinity of the gene phosphodiesterase 10A (PDE10A) on chromosome 6q27 (p = 1.7×10⁻⁸). 22205951 2011
dbSNP: rs650490
rs650490
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Polymorphic variants of 2q35-rs13387042, 3p24-rs4973768, 17q23-rs650490 and FGFR2-rs2981578 were analyzed to test for their association with breast cancer susceptibility. 22287734 2012
dbSNP: rs650490
rs650490
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Polymorphic variants of 2q35-rs13387042, 3p24-rs4973768, 17q23-rs650490 and FGFR2-rs2981578 were analyzed to test for their association with breast cancer susceptibility. 22287734 2012
dbSNP: rs778899140
rs778899140
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C3887506
Disease:
Hyperkinesia
0.010 GeneticVariation BEFREE Here, we report on germline PDE10A mutations in eight individuals from two families affected by a hyperkinetic movement disorder due to homozygous mutations c.320A>G (p.Tyr107Cys) and c.346G>C (p.Ala116Pro). 27058446 2016
dbSNP: rs778899140
rs778899140
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0424295
Disease:
Hyperactive behavior
0.010 GeneticVariation BEFREE Here, we report on germline PDE10A mutations in eight individuals from two families affected by a hyperkinetic movement disorder due to homozygous mutations c.320A>G (p.Tyr107Cys) and c.346G>C (p.Ala116Pro). 27058446 2016
dbSNP: rs875989839
rs875989839
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C3887506
Disease:
Hyperkinesia
0.010 GeneticVariation BEFREE Here, we report on germline PDE10A mutations in eight individuals from two families affected by a hyperkinetic movement disorder due to homozygous mutations c.320A>G (p.Tyr107Cys) and c.346G>C (p.Ala116Pro). 27058446 2016
dbSNP: rs875989839
rs875989839
Entrez Id: 10846
Gene Symbol: PDE10A
PDE10A
CUI: C0424295
Disease:
Hyperactive behavior
0.010 GeneticVariation BEFREE Here, we report on germline PDE10A mutations in eight individuals from two families affected by a hyperkinetic movement disorder due to homozygous mutations c.320A>G (p.Tyr107Cys) and c.346G>C (p.Ala116Pro). 27058446 2016