RAP1GAP, RAP1 GTPase activating protein, 5909

N. diseases: 63; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2275360
rs2275360
Entrez Id: 5909
Gene Symbol: RAP1GAP
RAP1GAP
CUI: C0523827
Disease:
Inorganic phosphate measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs2275360
rs2275360
Entrez Id: 5909
Gene Symbol: RAP1GAP
RAP1GAP
CUI: C0202178
Disease:
Phosphorus measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs77972946
rs77972946
Entrez Id: 5909
Gene Symbol: RAP1GAP
RAP1GAP
CUI: C0201850
Disease:
Alkaline phosphatase measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs829375
rs829375
Entrez Id: 5909
Gene Symbol: RAP1GAP
RAP1GAP
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs147394161
rs147394161
Entrez Id: 5909
Gene Symbol: RAP1GAP
RAP1GAP
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.700 GeneticVariation UNIPROT
dbSNP: rs147394161
rs147394161
Entrez Id: 5909
Gene Symbol: RAP1GAP
RAP1GAP
CUI: C0040136
Disease:
Thyroid Neoplasm 		0.010 GeneticVariation BEFREE A genetic polymorphism, Y609C, was seen in 7% of thyroid tumors but was not related to gene downregulation. 20124489 2010