Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16960027
rs16960027
Entrez Id: 29070;221191
Gene Symbol: CCDC113;PRSS54
CCDC113;PRSS54
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: rs16960035
rs16960035
Entrez Id: 29070;221191
Gene Symbol: CCDC113;PRSS54
CCDC113;PRSS54
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: rs17241091
rs17241091
Entrez Id: 29070;221191
Gene Symbol: CCDC113;PRSS54
CCDC113;PRSS54
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: rs2550374
rs2550374
Entrez Id: 29070
Gene Symbol: CCDC113
CCDC113
CUI: C0008312
Disease:
Primary biliary cirrhosis 		0.700 GeneticVariation GWASCAT A genome-wide association study identifies six novel risk loci for primary biliary cholangitis. 28425483 2017
dbSNP: rs2731763
rs2731763
Entrez Id: 29070;105371293
Gene Symbol: CCDC113;LOC105371293
CCDC113;LOC105371293
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic 		G 0.700 GeneticVariation GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469 2017
dbSNP: rs7193906
rs7193906
Entrez Id: 29070
Gene Symbol: CCDC113
CCDC113
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