ClinVar Miner

List of variants in gene LOC132089773, ODAD2 studied for Primary ciliary dyskinesia 23

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018076.5(ODAD2):c.3121G>T (p.Ala1041Ser) rs3737184 0.02212
NM_018076.5(ODAD2):c.3086C>T (p.Ser1029Phe) rs138588942 0.00108
NM_018076.5(ODAD2):c.3069T>C (p.Ala1023=) rs546928912 0.00011
NM_018076.5(ODAD2):c.3113C>G (p.Thr1038Arg) rs767489618 0.00001
NM_018076.5(ODAD2):c.3114A>C (p.Thr1038=) rs1379144760 0.00001
NM_018076.5(ODAD2):c.3129C>T (p.Tyr1043=) rs770927145 0.00001
NM_018076.5(ODAD2):c.3031_3037del (p.Asp1011fs) rs2132709474
NM_018076.5(ODAD2):c.3056A>T (p.Asp1019Val) rs772239137
NM_018076.5(ODAD2):c.3069T>G (p.Ala1023=)
NM_018076.5(ODAD2):c.3095G>A (p.Arg1032His) rs375622560

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.