SNX17, sorting nexin 17, 9784

N. diseases: 13; N. variants: 5
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: C0206161
Disease:
Reticulocyte count (procedure)
C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016