Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs142093111
rs142093111
Entrez Id: 4036
Gene Symbol: LRP2
LRP2
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
dbSNP: rs16856823
rs16856823
Entrez Id: 4036
Gene Symbol: LRP2
LRP2
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs200309784
rs200309784
Entrez Id: 4036
Gene Symbol: LRP2
LRP2
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
GA 0.700 GeneticVariation GWASCAT Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study. 29779033 2018
dbSNP: rs4667594
rs4667594
Entrez Id: 4036
Gene Symbol: LRP2
LRP2
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
A 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016