SNX5, sorting nexin 5, 27131

N. diseases: 24; N. variants: 3
Disease: Red Blood Cell Count measurement ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17802375
rs17802375
Entrez Id: 27131;58495
Gene Symbol: SNX5;OVOL2
SNX5;OVOL2
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019