rs1553511224, TBR1

N. diseases: 10
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Gait abnormality
CUI: C0575081
Disease: Gait abnormality
0.700 GeneticVariation CLINVAR
Inflexible adherence to routines or rituals
CUI: C1837653
Disease: Inflexible adherence to routines or rituals
0.700 GeneticVariation CLINVAR
Severe global developmental delay
CUI: C1837397
Disease: Severe global developmental delay
0.700 GeneticVariation CLINVAR
Cortical Dysplasia
CUI: C0431380
Disease: Cortical Dysplasia
0.700 GeneticVariation CLINVAR
Dysmorphic facies
CUI: C0424503
Disease: Dysmorphic facies
0.700 GeneticVariation CLINVAR
Electroencephalogram abnormal
CUI: C0151611
Disease: Electroencephalogram abnormal
0.700 GeneticVariation CLINVAR
Generalized hypotonia
CUI: C1858120
Disease: Generalized hypotonia
0.700 GeneticVariation CLINVAR
Hypoplastic hippocampus
CUI: C4476822
Disease: Hypoplastic hippocampus
0.700 GeneticVariation CLINVAR
Hypoplastic anterior commissure
CUI: C4022524
Disease: Hypoplastic anterior commissure
0.700 GeneticVariation CLINVAR
Absent speech
CUI: C1854882
Disease: Absent speech
0.700 GeneticVariation CLINVAR