Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11772848
rs11772848
Entrez Id: 136227
Gene Symbol: COL26A1
COL26A1
CUI: C0040420
Disease:
Tonometry 		G 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018
dbSNP: rs62465642
rs62465642
Entrez Id: 136227
Gene Symbol: COL26A1
COL26A1
CUI: C0040420
Disease:
Tonometry 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018
dbSNP: rs12532276
rs12532276
Entrez Id: 136227
Gene Symbol: COL26A1
COL26A1
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: rs17135414
rs17135414
Entrez Id: 136227
Gene Symbol: COL26A1
COL26A1
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: rs4727491
rs4727491
Entrez Id: 136227
Gene Symbol: COL26A1
COL26A1
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: rs4727491
rs4727491
Entrez Id: 136227
Gene Symbol: COL26A1
COL26A1
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: rs7782656
rs7782656
Entrez Id: 136227
Gene Symbol: COL26A1
COL26A1
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