rs1178187217, DNAH11

N. diseases: 38
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Spontaneous pneumothorax
CUI: C0149781
Disease: Spontaneous pneumothorax
0.700 GeneticVariation CLINVAR
CILIARY DYSKINESIA, PRIMARY, 7 (disorder)
CUI: C2678473
Disease: CILIARY DYSKINESIA, PRIMARY, 7 (disorder)
0.700 GeneticVariation CLINVAR
Rhinitis
CUI: C0035455
Disease: Rhinitis
0.700 GeneticVariation CLINVAR
Recurrent sinusitis
CUI: C0581354
Disease: Recurrent sinusitis
0.700 GeneticVariation CLINVAR
Headache
CUI: C0018681
Disease: Headache
0.700 GeneticVariation CLINVAR
Acute bronchitis
CUI: C0149514
Disease: Acute bronchitis
0.700 GeneticVariation CLINVAR
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
0.700 GeneticVariation CLINVAR
Acne
CUI: C0702166
Disease: Acne
0.700 GeneticVariation CLINVAR
Byzanthine arch palate
CUI: C0240635
Disease: Byzanthine arch palate
0.700 GeneticVariation CLINVAR
Hypoxemia
CUI: C0700292
Disease: Hypoxemia
0.700 GeneticVariation CLINVAR
Weight Gain
CUI: C0043094
Disease: Weight Gain
0.700 GeneticVariation CLINVAR
Chronic sinusitis
CUI: C0149516
Disease: Chronic sinusitis
0.700 GeneticVariation CLINVAR
Syncope
CUI: C0039070
Disease: Syncope
0.700 GeneticVariation CLINVAR
Dyspnea
CUI: C0013404
Disease: Dyspnea
0.700 GeneticVariation CLINVAR
Abnormality of the uvula
CUI: C4025885
Disease: Abnormality of the uvula
0.700 GeneticVariation CLINVAR
Pleurisy
CUI: C0032231
Disease: Pleurisy
0.700 GeneticVariation CLINVAR
Recurrent pneumonia
CUI: C0694550
Disease: Recurrent pneumonia
0.700 GeneticVariation CLINVAR
Asthma
CUI: C0004096
Disease: Asthma
0.700 GeneticVariation CLINVAR
Atelectasis
CUI: C0004144
Disease: Atelectasis
0.700 GeneticVariation CLINVAR
Chest Pain
CUI: C0008031
Disease: Chest Pain
0.700 GeneticVariation CLINVAR
Respiratory Depression
CUI: C0235063
Disease: Respiratory Depression
0.700 GeneticVariation CLINVAR
Large head (disorder)
CUI: C2243051
Disease: Large head (disorder)
0.700 GeneticVariation CLINVAR
Scoliosis, unspecified
CUI: C0036439
Disease: Scoliosis, unspecified
0.700 GeneticVariation CLINVAR
Melanocortin 4 Receptor Deficiency
CUI: C4054546
Disease: Melanocortin 4 Receptor Deficiency
0.700 GeneticVariation CLINVAR
Chronic lung disease
CUI: C0746102
Disease: Chronic lung disease
0.700 GeneticVariation CLINVAR