Neurodevelopmental Disorder with Cerebral Atrophy and Variable Facial Dysmorphism
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Associated Genes (1)
Associated Variants (7)
| RSID | Gene | Evidence |
|---|---|---|
| RS2138814108 | TTC5 | strong |
| RS1444869298 | TTC5 | strong |
| RS2138814053 | TTC5 | strong |
| RS199831317 | TTC5 | strong |
| RS749799203 | TTC5 | strong |
| RS769374125 | TTC5 | strong |
| RS552581393 | TTC5 | strong |