MECOM-AS1, MECOM antisense RNA 1, 105374205

N. diseases: 7; N. variants: 9
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1918973
rs1918973
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
CUI: C0001948
Disease:
Alcohol consumption 		A 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs1918973
rs1918973
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
CUI: C0428886
Disease:
Mean blood pressure 		A 0.700 GeneticVariation GWASCAT Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. 29912962 2018
dbSNP: rs73174306
rs73174306
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs12632583
rs12632583
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
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: rs1918976
rs1918976
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
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: rs3817581
rs3817581
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
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: rs3817581
rs3817581
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
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: rs4955659
rs4955659
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
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: rs10711289
rs10711289
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
CUI: C0018935
Disease:
Hematocrit procedure 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1343040
rs1343040
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
CUI: C0005823
Disease:
Blood Pressure 		0.700 GeneticVariation GWASDB Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. 21909110 2011
dbSNP: rs1918974
rs1918974
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282 2011
dbSNP: rs1918974
rs1918974
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
CUI: C1305849
Disease:
Diastolic blood pressure measurement 		T 0.700 GeneticVariation GWASDB Genome-wide association study identifies eight loci associated with blood pressure. 19430483 2009
dbSNP: rs1918974
rs1918974
Entrez Id: 2122;105374205
Gene Symbol: MECOM;MECOM-AS1
MECOM;MECOM-AS1
CUI: C0428883
Disease:
Diastolic blood pressure 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies eight loci associated with blood pressure. 19430483 2009