Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs781821239
rs781821239
B3GNT6
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood 		G 0.700 GeneticVariation CLINVAR De novo variants in sporadic cases of childhood onset schizophrenia. 26508570

2016