Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7970014
rs7970014
Entrez Id: 105370004
Gene Symbol: LINC02463
LINC02463
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: rs7977515
rs7977515
Entrez Id: 105370004
Gene Symbol: LINC02463
LINC02463
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: rs9989045
rs9989045
Entrez Id: 105370004
Gene Symbol: LINC02463
LINC02463
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: rs9989045
rs9989045
Entrez Id: 105370004
Gene Symbol: LINC02463
LINC02463
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: rs11067815
rs11067815
Entrez Id: 105370004
Gene Symbol: LINC02463
LINC02463
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394 2013
dbSNP: rs4767382
rs4767382
Entrez Id: 105370004
Gene Symbol: LINC02463
LINC02463
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394 2013
dbSNP: rs7964653
rs7964653
Entrez Id: 105370004
Gene Symbol: LINC02463
LINC02463
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394 2013
dbSNP: rs7967915
rs7967915
Entrez Id: 105370004
Gene Symbol: LINC02463
LINC02463
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB A genome-wide association study of a coronary artery disease risk variant. 23364394 2013