Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1007345781
rs1007345781
C 0.700 CausalMutation CLINVAR ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6. 23891469

2013

dbSNP: rs1034327724
rs1034327724
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060500990
rs1060500990
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501181
rs1060501181
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501454
rs1060501454
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501455
rs1060501455
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501456
rs1060501456
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501457
rs1060501457
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501458
rs1060501458
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501459
rs1060501459
CTA 0.700 CausalMutation CLINVAR

dbSNP: rs1060501460
rs1060501460
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
T 0.700 CausalMutation CLINVAR Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. 11788826

2002

dbSNP: rs1060501461
rs1060501461
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
C 0.700 CausalMutation CLINVAR Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. 11788826

2002

dbSNP: rs1060501464
rs1060501464
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060501466
rs1060501466
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060501467
rs1060501467
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060501719
rs1060501719
ACCG 0.700 CausalMutation CLINVAR

dbSNP: rs1060501861
rs1060501861
AT 0.700 CausalMutation CLINVAR

dbSNP: rs1060502202
rs1060502202
A 0.700 CausalMutation CLINVAR

dbSNP: rs1060502829
rs1060502829
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060502831
rs1060502831
GGCGTC 0.700 CausalMutation CLINVAR

dbSNP: rs1060503041
rs1060503041
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1060503063
rs1060503063
T 0.700 CausalMutation CLINVAR

dbSNP: rs1060503064
rs1060503064
C 0.700 GeneticVariation CLINVAR