rs1057518864, TCF4

N. diseases: 7
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Global developmental delay
CUI: C0557874
Disease: Global developmental delay
0.700 CausalMutation CLINVAR
Short nose
CUI: C1854114
Disease: Short nose
0.700 CausalMutation CLINVAR
Stereotypic Movement Disorder
CUI: C0038273
Disease: Stereotypic Movement Disorder
0.700 CausalMutation CLINVAR
Feeding difficulties in infancy
CUI: C2674608
Disease: Feeding difficulties in infancy
0.700 CausalMutation CLINVAR
Congenital Epicanthus
CUI: C0678230
Disease: Congenital Epicanthus
0.700 CausalMutation CLINVAR
Drooling
CUI: C0013132
Disease: Drooling
0.700 CausalMutation CLINVAR
Anteverted nostril
CUI: C1840077
Disease: Anteverted nostril
0.700 CausalMutation CLINVAR