rs1178187217, DNAH11

N. diseases: 38
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Pleural effusion disorder
CUI: C0032227
Disease: Pleural effusion disorder
14 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Pleurisy
CUI: C0032231
Disease: Pleurisy
7 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Premature Birth
CUI: C0151526
Disease: Premature Birth
50 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Recurrent otitis media
CUI: C0747085
Disease: Recurrent otitis media
11 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Recurrent pneumonia
CUI: C0694550
Disease: Recurrent pneumonia
11 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Recurrent sinusitis
CUI: C0581354
Disease: Recurrent sinusitis
3 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Respiratory Depression
CUI: C0235063
Disease: Respiratory Depression
5 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Rhinitis
CUI: C0035455
Disease: Rhinitis
20 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Scoliosis, unspecified
CUI: C0036439
Disease: Scoliosis, unspecified
135 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Spontaneous pneumothorax
CUI: C0149781
Disease: Spontaneous pneumothorax
6 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Syncope
CUI: C0039070
Disease: Syncope
45 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Tinnitus
CUI: C0040264
Disease: Tinnitus
14 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0
Weight Gain
CUI: C0043094
Disease: Weight Gain
12 0.683 0.480 7 21600085 missense variant G/A;T snv 4.3E-06 0.700 0