rs1163944538, TMEM94

N. diseases: 73
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Expressive language delay
CUI: C0454641
Disease: Expressive language delay
0.700 CausalMutation CLINVAR
Acid reflux
CUI: C4317146
Disease: Acid reflux
0.700 CausalMutation CLINVAR
Thoracolumbar scoliosis
CUI: C0749379
Disease: Thoracolumbar scoliosis
0.700 CausalMutation CLINVAR
Long eyelashes
CUI: C1853738
Disease: Long eyelashes
0.700 CausalMutation CLINVAR
Tall chin
CUI: C4021875
Disease: Tall chin
0.700 CausalMutation CLINVAR
Numerous nevi
CUI: C1849677
Disease: Numerous nevi
0.700 CausalMutation CLINVAR
Optic Nerve Glioma
CUI: C0346326
Disease: Optic Nerve Glioma
0.700 CausalMutation CLINVAR
Dysmorphic facies
CUI: C0424503
Disease: Dysmorphic facies
0.700 CausalMutation CLINVAR
Dyspnea on exertion
CUI: C0231807
Disease: Dyspnea on exertion
0.700 CausalMutation CLINVAR
Thick eyebrow
CUI: C1853487
Disease: Thick eyebrow
0.700 CausalMutation CLINVAR
Abnormality of the hip bone
CUI: C4021735
Disease: Abnormality of the hip bone
0.700 CausalMutation CLINVAR
Arnold Chiari Malformation
CUI: C0003803
Disease: Arnold Chiari Malformation
0.700 CausalMutation CLINVAR
Hypoplastic helices
CUI: C1842681
Disease: Hypoplastic helices
0.700 CausalMutation CLINVAR
Poor school performance
CUI: C1843367
Disease: Poor school performance
0.700 CausalMutation CLINVAR
Premature Birth
CUI: C0151526
Disease: Premature Birth
0.700 CausalMutation CLINVAR
Specific learning disability
CUI: C4025790
Disease: Specific learning disability
0.700 CausalMutation CLINVAR
Cerebral Hemorrhage
CUI: C2937358
Disease: Cerebral Hemorrhage
0.700 CausalMutation CLINVAR
Recurrent pneumonia
CUI: C0694550
Disease: Recurrent pneumonia
0.700 CausalMutation CLINVAR
Single transverse palmar crease
CUI: C0424731
Disease: Single transverse palmar crease
0.700 CausalMutation CLINVAR
Patent ductus arteriosus
CUI: C0013274
Disease: Patent ductus arteriosus
0.700 CausalMutation CLINVAR
Cartilaginous exostosis
CUI: C0029423
Disease: Cartilaginous exostosis
0.700 CausalMutation CLINVAR
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
0.700 CausalMutation CLINVAR
Muscle hypotonia
CUI: C0026827
Disease: Muscle hypotonia
0.700 CausalMutation CLINVAR
Sinus Tachycardia
CUI: C0039239
Disease: Sinus Tachycardia
0.700 CausalMutation CLINVAR
Byzanthine arch palate
CUI: C0240635
Disease: Byzanthine arch palate
0.700 CausalMutation CLINVAR