CTNNA1, catenin alpha 1, 1495

N. diseases: 82; N. variants: 35
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs755215402
rs755215402
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
CUI: C1837029
Disease:
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 		0.800 GeneticVariation UNIPROT Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity. 26691986 2016
dbSNP: rs869320696
rs869320696
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
CUI: C1837029
Disease:
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 		0.800 GeneticVariation UNIPROT Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity. 26691986 2016
dbSNP: rs869320697
rs869320697
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
CUI: C1837029
Disease:
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 		0.800 GeneticVariation UNIPROT Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity. 26691986 2016
dbSNP: rs755215402
rs755215402
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
CUI: C1837029
Disease:
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 		G 0.800 CausalMutation CLINVAR
dbSNP: rs869320696
rs869320696
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
CUI: C1837029
Disease:
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 		C 0.800 CausalMutation CLINVAR
dbSNP: rs869320697
rs869320697
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
CUI: C1837029
Disease:
Macular Dystrophy, Butterfly-Shaped Pigmentary, 2 		A 0.800 CausalMutation CLINVAR
dbSNP: rs10038162
rs10038162
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs10043478
rs10043478
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs10515504
rs10515504
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs11744283
rs11744283
Entrez Id: 1495;26045
Gene Symbol: CTNNA1;LRRTM2
CTNNA1;LRRTM2
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: rs11749163
rs11749163
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs13171173
rs13171173
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs13177415
rs13177415
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs160399
rs160399
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs160400
rs160400
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs160401
rs160401
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs160404
rs160404
Entrez Id: 1495;105379194
Gene Symbol: CTNNA1;LOC105379194
CTNNA1;LOC105379194
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: rs160405
rs160405
Entrez Id: 1495;105379194
Gene Symbol: CTNNA1;LOC105379194
CTNNA1;LOC105379194
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: rs1651358
rs1651358
Entrez Id: 1495;105379194
Gene Symbol: CTNNA1;LOC105379194
CTNNA1;LOC105379194
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: rs17031
rs17031
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs17207681
rs17207681
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs17286171
rs17286171
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs176382
rs176382
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs1828187
rs1828187
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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: rs288016
rs288016
Entrez Id: 1495
Gene Symbol: CTNNA1
CTNNA1
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