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rs13194053

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs13194053(C;C)
Make rs13194053(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position27176104
GeneTRNAI20
is asnp
is mentioned by
dbSNPrs13194053
ebirs13194053
HLIrs13194053
Exacrs13194053
Varsomers13194053
Maprs13194053
PheGenIrs13194053
hapmaprs13194053
1000 genomesrs13194053
hgdprs13194053
ensemblrs13194053
gopubmedrs13194053
geneviewrs13194053
scholarrs13194053
googlers13194053
pharmgkbrs13194053
gwascentralrs13194053
openSNPrs13194053
23andMers13194053
23andMe allrs13194053
SNP Nexus

SNPshotrs13194053
SNPdbers13194053
MSV3drs13194053
GWAS Ctlgrs13194053
GMAF0.1061
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19571809OA-icon.png]
Trait Schizophrenia
Title Common variants on chromosome 6p22.1 are associated with schizophrenia
Risk Allele T
P-val 1E-8
Odds Ratio 1.28 [NR]
GWAS snp
PMID [PMID 19571811OA-icon.png]
Trait Schizophrenia
Title Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
Risk Allele T
P-val 1E-8
Odds Ratio 1.22 None
OMIM181500
Desc
Variant
Relatedalso
[PMID 19911060OA-icon.png] Persistence criteria for susceptibility genes for schizophrenia: a discussion from an evolutionary viewpoint.


[PMID 20485477OA-icon.png] New Genetic Findings in Schizophrenia: Is there Still Room for the Dopamine Hypothesis of Schizophrenia?


GET Evidence
rs13194053
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.125
summary



[PMID 22005930OA-icon.png] Genome-wide association study of Alzheimer's disease with psychotic symptoms.