rs749203329, MLLT1

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Cerebral atrophy
CUI: C0235946
Disease: Cerebral atrophy
0.700 GeneticVariation CLINVAR
Infantile Spasm
CUI: C3887898
Disease: Infantile Spasm
0.700 GeneticVariation CLINVAR
Abnormal cortical gyration
CUI: C1856019
Disease: Abnormal cortical gyration
0.700 GeneticVariation CLINVAR
Short nose
CUI: C1854114
Disease: Short nose
0.700 GeneticVariation CLINVAR
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 GeneticVariation CLINVAR
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
0.700 GeneticVariation CLINVAR
Orbital separation excessive
CUI: C0020534
Disease: Orbital separation excessive
0.700 GeneticVariation CLINVAR