Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863223355
rs863223355
RYR2
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood 		C 0.700 GeneticVariation CLINVAR De novo variants in sporadic cases of childhood onset schizophrenia. 26508570

2016