ZNF568, zinc finger protein 568, 374900

N. diseases: 4; N. variants: 3
Disease: Child Development Disorders, Pervasive ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs138867053
rs138867053
Entrez Id: 374900
Gene Symbol: ZNF568
ZNF568
CUI: C0008074
Disease:
Child Development Disorders, Pervasive 		A 0.700 GeneticVariation GWASCAT Identification of common genetic risk variants for autism spectrum disorder. 30804558 2019