rs6277, DRD2

N. diseases: 36
Disease: Stuttering ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Stuttering
CUI: C0038506
Disease: Stuttering
0.020 GeneticVariation BEFREE The allele frequencies of DRD2 C957T were not significantly different between the CWS and the CWNS; however, the frequency of the TT genotype was significantly higher among the CWS (p = 0.02), which was associated with 2.25-fold susceptibility to stuttering (OR = 2.25, 95% CI = 1.03 to 4.90, p = 0.04). 30199750 2019
Stuttering
CUI: C0038506
Disease: Stuttering
0.020 GeneticVariation BEFREE This idea is supported by an additional path model showing that the polymorphism DRD2 C957T influences the self-reported severity of stuttering mainly by its influence on neuroticism (independent of the variable sex). 22262089 2012