Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3132581
rs3132581
Entrez Id: 135656;389376;102723346
Gene Symbol: MUCL3;SFTA2;HCG21
MUCL3;SFTA2;HCG21
CUI: C0008074
Disease:
Child Development Disorders, Pervasive
G 0.700 GeneticVariation GWASCAT Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. 23453885 2013