rs1555740650, PRR12

N. diseases: 13
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Exotropia
CUI: C0015310
Disease: Exotropia
0.700 CausalMutation CLINVAR
Pediatric failure to thrive
CUI: C2315100
Disease: Pediatric failure to thrive
0.700 CausalMutation CLINVAR
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
0.700 CausalMutation CLINVAR
Dysmorphic features
CUI: C0432072
Disease: Dysmorphic features
0.700 CausalMutation CLINVAR
Structural brain abnormalities
CUI: C1866933
Disease: Structural brain abnormalities
0.700 CausalMutation CLINVAR
Motor delay
CUI: C1854301
Disease: Motor delay
0.700 CausalMutation CLINVAR
Coloboma of iris
CUI: C0240063
Disease: Coloboma of iris
0.700 CausalMutation CLINVAR
Premature Birth
CUI: C0151526
Disease: Premature Birth
0.700 CausalMutation CLINVAR
Delayed speech and language development
CUI: C0454644
Disease: Delayed speech and language development
0.700 CausalMutation CLINVAR
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
0.700 CausalMutation CLINVAR
Microcephaly (physical finding)
CUI: C4551563
Disease: Microcephaly (physical finding)
0.700 CausalMutation CLINVAR
Gait abnormality
CUI: C0575081
Disease: Gait abnormality
0.700 CausalMutation CLINVAR
Abnormality of vision
CUI: C4025846
Disease: Abnormality of vision
0.700 CausalMutation CLINVAR