Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35186465
rs35186465
Entrez Id: 101928104
Gene Symbol: LINC01482
LINC01482
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: rs35186465
rs35186465
Entrez Id: 101928104
Gene Symbol: LINC01482
LINC01482
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: rs929477
rs929477
Entrez Id: 101928104
Gene Symbol: LINC01482
LINC01482
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs587776911
rs587776911
Entrez Id: 54757;101928104
Gene Symbol: FAM20A;LINC01482
FAM20A;LINC01482
CUI: C2931783
Disease:
Amelogenesis imperfecta nephrocalcinosis 		C 0.700 CausalMutation CLINVAR