KIAA0513, KIAA0513, 9764

N. diseases: 8; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8056742
rs8056742
Entrez Id: 9764
Gene Symbol: KIAA0513
KIAA0513
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis 		C 0.800 GeneticVariation GWASDB Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. 22959728 2013
dbSNP: rs8056742
rs8056742
Entrez Id: 9764
Gene Symbol: KIAA0513
KIAA0513
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis 		C 0.800 GeneticVariation GWASCAT Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. 22959728 2013
dbSNP: rs41337248
rs41337248
Entrez Id: 9764
Gene Symbol: KIAA0513
KIAA0513
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs41337248
rs41337248
Entrez Id: 9764
Gene Symbol: KIAA0513
KIAA0513
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs12446708
rs12446708
Entrez Id: 9764;105371380
Gene Symbol: KIAA0513;LOC105371380
KIAA0513;LOC105371380
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: rs12596553
rs12596553
Entrez Id: 9764
Gene Symbol: KIAA0513
KIAA0513
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: rs12932076
rs12932076
Entrez Id: 9764
Gene Symbol: KIAA0513
KIAA0513
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: rs16975185
rs16975185
Entrez Id: 9764
Gene Symbol: KIAA0513
KIAA0513
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: rs17789174
rs17789174
Entrez Id: 9764
Gene Symbol: KIAA0513
KIAA0513
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: rs3794679
rs3794679
Entrez Id: 9764
Gene Symbol: KIAA0513
KIAA0513
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: rs7196620
rs7196620
Entrez Id: 9764;105371380
Gene Symbol: KIAA0513;LOC105371380
KIAA0513;LOC105371380
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