CCDC39, coiled-coil domain containing 39, 339829

N. diseases: 56; N. variants: 49
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6782299
rs6782299
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
CUI: C0036341
Disease:
Schizophrenia 		T 0.800 GeneticVariation GWASCAT Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. 19571811 2009
dbSNP: rs6782299
rs6782299
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
CUI: C0036341
Disease:
Schizophrenia 		T 0.800 GeneticVariation GWASDB Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. 19571811 2009
dbSNP: rs10937044
rs10937044
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
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: rs11916345
rs11916345
Entrez Id: 339829;101928882;105374240
Gene Symbol: CCDC39;LOC101928882;LOC105374240
CCDC39;LOC101928882;LOC105374240
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: rs12497997
rs12497997
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
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: rs13069244
rs13069244
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
CUI: C0037369
Disease:
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
dbSNP: rs13069244
rs13069244
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
dbSNP: rs13073010
rs13073010
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
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: rs1401974
rs1401974
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
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: rs2037370
rs2037370
Entrez Id: 8087;339829;101928882;105374240
Gene Symbol: FXR1;CCDC39;LOC101928882;LOC105374240
FXR1;CCDC39;LOC101928882;LOC105374240
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: rs2338576
rs2338576
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
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: rs2338577
rs2338577
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
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: rs6782299
rs6782299
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
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: rs7617511
rs7617511
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
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: rs7643631
rs7643631
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
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: rs9838229
rs9838229
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
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: rs9838229
rs9838229
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
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: rs9838828
rs9838828
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
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: rs9858253
rs9858253
Entrez Id: 339829;101928882
Gene Symbol: CCDC39;LOC101928882
CCDC39;LOC101928882
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: rs587778820
rs587778820
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
CUI: C0008780
Disease:
Ciliary Motility Disorders 		C 0.700 CausalMutation CLINVAR Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel: Molecular and Clinical Findings in Italian Patients. 27637300 2016
dbSNP: rs201780665
rs201780665
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
CUI: C0008780
Disease:
Ciliary Motility Disorders 		A 0.700 CausalMutation CLINVAR The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesia. 24498942 2014
dbSNP: rs587778822
rs587778822
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
CUI: C0008780
Disease:
Ciliary Motility Disorders 		G 0.700 CausalMutation CLINVAR Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia. 25186273 2014
dbSNP: rs773801386
rs773801386
Entrez Id: 339829
Gene Symbol: CCDC39
CCDC39
CUI: C3151136
Disease:
CILIARY DYSKINESIA, PRIMARY, 14 		C 0.700 GeneticVariation CLINVAR The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesia. 24498942 2014
dbSNP: rs1007345781
rs1007345781
Entrez Id: 151613;339829
Gene Symbol: TTC14;CCDC39
TTC14;CCDC39
CUI: C0008780
Disease:
Ciliary Motility Disorders 		C 0.700 CausalMutation CLINVAR ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. 23891469 2013
dbSNP: rs1560079213
rs1560079213
Entrez Id: 151613;339829
Gene Symbol: TTC14;CCDC39
TTC14;CCDC39
CUI: C0008780
Disease:
Ciliary Motility Disorders 		C 0.700 GeneticVariation CLINVAR Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms. 23255504 2013