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| Deafness_Isolated v0.182 | SNAI2 | Zornitza Stark Marked gene: SNAI2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.182 | SNAI2 | Zornitza Stark Gene: snai2 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_Isolated v0.0 | SNAI2 |
Zornitza Stark gene: SNAI2 was added gene: SNAI2 was added to DeafnessIsolated. Sources: Expert Review Amber,Melbourne Genomics Health Alliance Deafness Flagship,Victorian Clinical Genetics Services Mode of inheritance for gene: SNAI2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SNAI2 were set to 30936914; 12444107 Phenotypes for gene: SNAI2 were set to Waardenburg syndrome, type 2D, MIM# 608890 |
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