rs1559931177, QRICH1

N. diseases: 34
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Birth length less than 3rd percentile
0.700 CausalMutation CLINVAR
Delayed speech and language development
0.700 CausalMutation CLINVAR
Broad-based gait
CUI: C0856863
Disease: Broad-based gait
0.700 CausalMutation CLINVAR
Fatigue
CUI: C0015672
Disease: Fatigue
0.700 CausalMutation CLINVAR
Prolonged neonatal jaundice
CUI: C1859236
Disease: Prolonged neonatal jaundice
0.700 CausalMutation CLINVAR
Peripheral Neuropathy
CUI: C0031117
Disease: Peripheral Neuropathy
0.700 CausalMutation CLINVAR
Myopathic facies
CUI: C0332615
Disease: Myopathic facies
0.700 CausalMutation CLINVAR
Sleep Apnea, Central
CUI: C0520680
Disease: Sleep Apnea, Central
0.700 CausalMutation CLINVAR
Small for gestational age (disorder)
0.700 CausalMutation CLINVAR