Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1106766
rs1106766
Entrez Id: 22864
Gene Symbol: R3HDM2
R3HDM2
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016