WDR59
HGNC:25706 · SaudiVarKB evidence summary derived from retained literature mentions.
2Gene mentions
2Publications
2Linked variants
3Associated phenotypes
Associated phenotypes
Co-mentioned in WDR59 publications| Phenotype | Identifier | Articles | Mentions |
|---|---|---|---|
| cardiomyopathy | HP:0001638 | 1 | 1 |
| intellectual disability | HP:0001249 | 1 | 1 |
| developmental delay | HP:0001263 | 1 | 1 |
Linked variants
Variants normalized to WDR59| Variant | HGVS / rsID | Articles | Mentions |
|---|---|---|---|
| c.2887G>A | c.2887G>A | 1 | 1 |
| p.Gly963Arg | p.Gly963Arg | 1 | 1 |
Population context
Reported in the same publications| Country / region | Group | Cohort | Articles |
|---|---|---|---|
| Saudi Arabia | — | — | 1 |
| Saudi Arabia | — | 1,000 | 1 |