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| Deafness_Isolated v0.182 | CACNA1D | Zornitza Stark Marked gene: CACNA1D as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.182 | CACNA1D | Zornitza Stark Gene: cacna1d has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.0 | CACNA1D |
Zornitza Stark gene: CACNA1D was added gene: CACNA1D was added to DeafnessIsolated. Sources: Expert Review Amber,Melbourne Genomics Health Alliance Deafness Flagship,Victorian Clinical Genetics Services Mode of inheritance for gene: CACNA1D was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CACNA1D were set to 21131953; 15357422; 22678062 Phenotypes for gene: CACNA1D were set to Sinoatrial node dysfunction and deafness, MIM# 614896 |
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