Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1561117442
rs1561117442
5 55226917 frameshift variant C/- delins
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases 0.700 0
dbSNP: rs777031813
rs777031813
1.000 0.160 5 55222341 stop gained G/A;T snv 3.0E-05; 7.5E-06
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs797045151
rs797045151
1.000 0.160 5 55220427 missense variant C/T snv
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases 0.700 0
dbSNP: rs797045152
rs797045152
1.000 0.160 5 55220382 missense variant C/A;T snv
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases; Cardiovascular Diseases 0.700 0