SNX17, sorting nexin 17, 9784

N. diseases: 13; N. variants: 5
Disease: Microalbuminuria ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4665972
rs4665972
Entrez Id: 9784
Gene Symbol: SNX17
SNX17
CUI: C0730345
Disease:
Microalbuminuria 		T 0.700 GeneticVariation GWASCAT Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. 31511532 2019