Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4765905
rs4765905
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.830 GeneticVariation BEFREE Three SNPs (rs1625579, rs1344706 and rs4765905) showed a consistent direction of effect with previous studies and the polygenic risk score constructed using the weighted sum of these three SNPs showed a significant association with Schizophrenia in this population (OR=3.78, p=0.005). 29599094

2018

dbSNP: rs4765905
rs4765905
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.830 GeneticVariation BEFREE Further analysis of the haplotype rs1006737-rs4765905-rs882194 in CACNA1C showed significant associations with schizophrenia (corrected global p<0.005), and two haplotypes (ACC and ACT) in the block were significantly increased in the patients. 24275578

2014

dbSNP: rs4765905
rs4765905
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.830 GeneticVariation BEFREE A history of suicide attempt was assessed in a sample of 1009 patients with BD, SCZ and related psychosis spectrum disorders, and associations with the joint genetic risk variants for BD and SCZ (rs2239547 (ITIH3/4-region), rs10994359 (ANK3) and rs4765905 (CACNA1C)) were investigated. 24461634

2014