Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12807809
rs12807809 		0.720 GeneticVariation BEFREE Minor allele C of rs12807809 polymorphism in NRGN contributes to the severity of psychosis in patients with Schizophrenia in South Indian population. 28389239

2017
dbSNP: rs12807809
rs12807809 		0.720 GeneticVariation BEFREE Despite the association between NRGN and psychoses we have found, we failed to validate the positive variant rs12807809, which was reported in the Caucasian genome-wide association study both in our single site association test and the meta-analysis. 26828755

2016
dbSNP: rs12807809
rs12807809 		0.720 GeneticVariation GWASDB Common variant at 16p11.2 conferring risk of psychosis. 23164818

2014