Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13131918
rs13131918
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
CUI: C0202236
Disease:
Triglycerides measurement 		0.700 GeneticVariation GWASCAT Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels. 30255771 2018
dbSNP: rs137945355
rs137945355
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		0.700 GeneticVariation GWASCAT Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. 28736931 2018
dbSNP: rs1122594
rs1122594
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
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: rs1122594
rs1122594
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
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: rs11721701
rs11721701
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
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: rs11943001
rs11943001
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
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: rs41421648
rs41421648
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
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: rs534951121
rs534951121
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
CUI: C0424678
Disease:
Lean body mass 		T 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs7656118
rs7656118
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
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: rs7680589
rs7680589
Entrez Id: 91050
Gene Symbol: CCDC149
CCDC149
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