{{Rsnum
|rsid=175174
|Gene=ZDHHC8
|Chromosome=22
|position=20140031
|Orientation=plus
|GMAF=0.4949
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ZDHHC8
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 41.1 | 38.4 | 20.5
| HCB | 12.4 | 39.4 | 48.2
| JPT | 17.1 | 42.3 | 40.5
| YRI | 21.1 | 51.0 | 27.9
| ASW | 21.1 | 52.6 | 26.3
| CHB | 12.4 | 39.4 | 48.2
| CHD | 11.0 | 43.1 | 45.9
| GIH | 21.8 | 57.4 | 20.8
| LWK | 31.8 | 52.7 | 15.5
| MEX | 20.7 | 51.7 | 27.6
| MKK | 34.0 | 50.6 | 15.4
| TSI | 45.1 | 42.2 | 12.7
| HapMapRevision=28
}}This snp in the gene [[ZDHHC8]] does not appear to have any link to [[schizophrenia]] despite being quite [[popular in pubmed]]

{{omim
|desc=SCHIZOPHRENIA; SCZD
|id=181500
|rsnum=175174
}}

{{omim
|desc=ZINC FINGER DHHC DOMAIN-CONTAINING PROTEIN 8; ZDHHC8
|id=608784
|rsnum=175174
}}

{{PMID Auto
|PMID=15184899
|Title=Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia.
}}

{{PMID Auto
|PMID=15489219
|Title=Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8.
}}

{{PMID Auto
|PMID=15631889
|Title=No association was found between a functional SNP in ZDHHC8 and schizophrenia in a Japanese case-control population.
}}

{{PMID Auto
|PMID=15992527
|Title=No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples.
}}

{{PMID Auto
|PMID=16150541
|Title=The ZDHHC8 gene did not associate with bipolar disorder or schizophrenia.
}}

{{PMID Auto
|PMID=16225675
|Title=ZDHHC8 as a candidate gene for schizophrenia: analysis of a putative functional intronic marker in case-control and family-based association studies.
|OA=1
}}

{{PMID Auto
|PMID=16860541
|Title=Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.
}}

{{PMID Auto
|PMID=17622328
|Title=Analysis of TBX1 variation in patients with psychotic and affective disorders.
|OA=1
}}

{{PMID Auto
|PMID=17728672
|Title=ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia.
}}

{{PMID Auto
|PMID=18075473
|Title=HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention.
}}

{{PMID Auto
|PMID=19197363
|Title=A genome-wide investigation of SNPs and CNVs in schizophrenia.
|OA=1
}}

{{PMID Auto
|PMID=20661937
|Title=Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets.
}}

{{PMID Auto
|PMID=23403413
|Title=ZDHHC8 gene may play a role in cortical volumes of patients with schizophrenia
}}

{{PMID Auto
|PMID=22763378
|Title=Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}