|?||(A;A) (A;G) (G;G)||28|
This snp in the gene ZDHHC8 does not appear to have any link to schizophrenia despite being quite popular in pubmed
[PMID 15184899] Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia.
[PMID 15489219] Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8.
[PMID 15631889] No association was found between a functional SNP in ZDHHC8 and schizophrenia in a Japanese case-control population.
[PMID 15992527] No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples.
[PMID 16150541] The ZDHHC8 gene did not associate with bipolar disorder or schizophrenia.
[PMID 16225675] ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies.
[PMID 16860541] Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.
[PMID 17622328] Analysis of TBX1 variation in patients with psychotic and affective disorders.
[PMID 17728672] ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia.
[PMID 18075473] HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention.
[PMID 19197363] A genome-wide investigation of SNPs and CNVs in schizophrenia.
[PMID 20661937] Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets.
[PMID 23403413] ZDHHC8 gene may play a role in cortical volumes of patients with schizophrenia
[PMID 22763378] Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.