Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060501454
rs1060501454
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501455
rs1060501455
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501456
rs1060501456
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501457
rs1060501457
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501458
rs1060501458
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501459
rs1060501459
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
CTA 0.700 CausalMutation CLINVAR

dbSNP: rs1060501460
rs1060501460
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
T 0.700 CausalMutation CLINVAR DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects. 16627867

2006

dbSNP: rs1060501460
rs1060501460
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
T 0.700 CausalMutation CLINVAR Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. 11788826

2002

dbSNP: rs1060501461
rs1060501461
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
C 0.700 CausalMutation CLINVAR DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects. 16627867

2006

dbSNP: rs1060501461
rs1060501461
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
C 0.700 CausalMutation CLINVAR Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. 11788826

2002

dbSNP: rs1060501464
rs1060501464
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501466
rs1060501466
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501467
rs1060501467
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
T 0.700 CausalMutation CLINVAR

dbSNP: rs116128702
rs116128702
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR

dbSNP: rs1161303371
rs1161303371
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
G 0.700 CausalMutation CLINVAR An effective combination of sanger and next generation sequencing in diagnostics of primary ciliary dyskinesia. 26228299

2016

dbSNP: rs1175877764
rs1175877764
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR

dbSNP: rs1188507108
rs1188507108
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR

dbSNP: rs1193586811
rs1193586811
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects. 16627867

2006

dbSNP: rs1273352530
rs1273352530
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR

dbSNP: rs1283070426
rs1283070426
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR

dbSNP: rs1304504006
rs1304504006
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 GeneticVariation CLINVAR ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. 23891469

2013

dbSNP: rs1304504006
rs1304504006
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 GeneticVariation CLINVAR Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia. 19357118

2009

dbSNP: rs1305797678
rs1305797678
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
G 0.700 GeneticVariation CLINVAR The prevalence of clinical features associated with primary ciliary dyskinesia in a heterotaxy population: results of a web-based survey. 24905662

2015

dbSNP: rs1353723750
rs1353723750
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
G 0.700 CausalMutation CLINVAR

dbSNP: rs1354919632
rs1354919632
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
A 0.700 CausalMutation CLINVAR