Disease: Pervasive Development Disorder ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12037377
rs12037377
Entrez Id: 64216
Gene Symbol: TFB2M
TFB2M
CUI: C0524528
Disease:
Pervasive Development Disorder 		0.010 GeneticVariation BEFREE Identification of a rare homozygous c.790C>T variation in the TFB2M gene in Korean patients with autism spectrum disorder. 30414672 2018