Disease: Albuminuria ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34823645
rs34823645
Entrez Id: 56918
Gene Symbol: C2orf83
C2orf83
CUI: C0001925
Disease:
Albuminuria 		C 0.700 GeneticVariation GWASCAT Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion. 30910378 2019