DCLK1, doublecortin like kinase 1, 9201

N. diseases: 123; N. variants: 17
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs138712069
rs138712069
Entrez Id: 9201;105370163
Gene Symbol: DCLK1;LOC105370163
DCLK1;LOC105370163
CUI: C0149782
Disease:
Squamous cell carcinoma of lung 		T 0.700 GeneticVariation GWASCAT Genome-wide association study of familial lung cancer. 29924316 2018
dbSNP: rs6563164
rs6563164
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs73176188
rs73176188
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs8000101
rs8000101
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs1171052
rs1171052
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
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: rs1171072
rs1171072
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
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: rs1171091
rs1171091
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
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: rs1171092
rs1171092
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
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: rs7319248
rs7319248
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
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: rs7358881
rs7358881
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
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: rs9565689
rs9565689
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
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: rs9574926
rs9574926
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
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: rs9593571
rs9593571
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
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: rs6563210
rs6563210
Entrez Id: 9201;105370163
Gene Symbol: DCLK1;LOC105370163
DCLK1;LOC105370163
CUI: C0489786
Disease:
Height 		A 0.700 GeneticVariation GWASDB Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry. 21998595 2011
dbSNP: rs6563210
rs6563210
Entrez Id: 9201;105370163
Gene Symbol: DCLK1;LOC105370163
DCLK1;LOC105370163
CUI: C0005890
Disease:
Body Height 		A 0.700 GeneticVariation GWASCAT Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry. 21998595 2011
dbSNP: rs1366698690
rs1366698690
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
CUI: C0278701
Disease:
Gastric Adenocarcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs1926320
rs1926320
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
CUI: C0152136
Disease:
Low Tension Glaucoma 		0.010 GeneticVariation BEFREE Although the rs10483727 (SIX1), rs1926320 (DCLK1), or rs12025126 (RERE) alone may not be sufficient for the development of POAG, the association of these SNPs with a phenotypic feature in patients with NTG or HTG suggests that these loci contribute to the pathogenesis of POAG. 22584021 2012
dbSNP: rs1926320
rs1926320
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
CUI: C0339573
Disease:
Glaucoma, Primary Open Angle 		0.010 GeneticVariation BEFREE Although the rs10483727 (SIX1), rs1926320 (DCLK1), or rs12025126 (RERE) alone may not be sufficient for the development of POAG, the association of these SNPs with a phenotypic feature in patients with NTG or HTG suggests that these loci contribute to the pathogenesis of POAG. 22584021 2012
dbSNP: rs7989807
rs7989807
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder 		0.010 GeneticVariation BEFREE The main effect was observed for rs7989807 in intron 3, which was strongly associated with SCZ alone and even more so when cases with SCZ and ADHD were combined (P-value = 4 × 10(-5) and 4 × 10(-6), respectively). 22539971 2012
dbSNP: rs7989807
rs7989807
Entrez Id: 9201
Gene Symbol: DCLK1
DCLK1
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE The main effect was observed for rs7989807 in intron 3, which was strongly associated with SCZ alone and even more so when cases with SCZ and ADHD were combined (P-value = 4 × 10(-5) and 4 × 10(-6), respectively). 22539971 2012