| Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
|---|---|---|---|---|---|---|---|---|---|---|
|
G | 0.700 | CausalMutation | CLINVAR | ||||||
|
G | 0.700 | CausalMutation | CLINVAR | An effective combination of sanger and next generation sequencing in diagnostics of primary ciliary dyskinesia. | 26228299 | 2016 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
G | 0.700 | CausalMutation | CLINVAR | Ciliary beat pattern and frequency in genetic variants of primary ciliary dyskinesia. | 25186273 | 2014 |
|||
|
T | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | GeneticVariation | CLINVAR | DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects. | 16627867 | 2006 |
|||
|
C | 0.700 | GeneticVariation | CLINVAR | Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. | 11788826 | 2002 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia. | 19357118 | 2009 |
|||
|
A | 0.700 | CausalMutation | CLINVAR | DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects. | 16627867 | 2006 |
|||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
CT | 0.700 | CausalMutation | CLINVAR | ||||||
|
T | 0.700 | GeneticVariation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
CG | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
CT | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
C | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
A | 0.700 | CausalMutation | CLINVAR | ||||||
|
GT | 0.700 | CausalMutation | CLINVAR |