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rs175174

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 0
Make rs175174(A;A)
Make rs175174(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position20140031
GeneZDHHC8
is asnp
is mentioned by
dbSNPrs175174
ebirs175174
HLIrs175174
Exacrs175174
Varsomers175174
Maprs175174
PheGenIrs175174
hapmaprs175174
1000 genomesrs175174
hgdprs175174
ensemblrs175174
gopubmedrs175174
geneviewrs175174
scholarrs175174
googlers175174
pharmgkbrs175174
gwascentralrs175174
openSNPrs175174
23andMers175174
23andMe allrs175174
SNP Nexus

SNPshotrs175174
SNPdbers175174
MSV3drs175174
GWAS Ctlgrs175174
GMAF0.4949
Max Magnitude0
? (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
OMIM181500
DescSCHIZOPHRENIA; SCZD
Variant
Relatedalso
OMIM608784
DescZINC FINGER DHHC DOMAIN-CONTAINING PROTEIN 8; ZDHHC8
Variant
Relatedalso


[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 16225675OA-icon.png] 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 17622328OA-icon.png] 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 19197363OA-icon.png] 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 22763378OA-icon.png] Increased corpus callosum volume in children with chromosome 22q11.2 deletion syndrome is associated with neurocognitive deficits and genetic polymorphisms.