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rs10917670

From SNPedia

Orientationplus
Stabilizedplus
Make rs10917670(C;C)
Make rs10917670(C;T)
Make rs10917670(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position163063052
is asnp
is mentioned by
dbSNPrs10917670
ebirs10917670
HLIrs10917670
Exacrs10917670
Varsomers10917670
Maprs10917670
PheGenIrs10917670
hapmaprs10917670
1000 genomesrs10917670
hgdprs10917670
ensemblrs10917670
gopubmedrs10917670
geneviewrs10917670
scholarrs10917670
googlers10917670
pharmgkbrs10917670
gwascentralrs10917670
openSNPrs10917670
23andMers10917670
23andMe allrs10917670
SNP Nexus

SNPshotrs10917670
SNPdbers10917670
MSV3drs10917670
GWAS Ctlgrs10917670
GMAF0.4357
Max Magnitude

[PMID 19937977] Association study of NRG1, DTNBP1, RGS4, G72/G30, and PIP5K2A with schizophrenia and symptom severity in a Hungarian sample

[PMID 19282471OA-icon.png] RGS4 polymorphisms associated with variability of cognitive performance in a family-based schizophrenia sample


[PMID 16905560] RGS4 mRNA expression in postmortem human cortex is associated with COMT Val158Met genotype and COMT enzyme activity.


[PMID 17092693] RGS4 is not a susceptibility gene for schizophrenia in Japanese: association study in a large case-control population.


[PMID 18804346OA-icon.png] Interaction between interleukin 3 and dystrobrevin-binding protein 1 in schizophrenia.


[PMID 18834502OA-icon.png] Association of RGS4 variants with schizotypy and cognitive endophenotypes at the population level.


GET Evidence
rs10917670
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.460938
summary