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| Hereditary Neuropathy v2.0 | VWA1_HMNMYO_GCGCGGAGCG | STR VWA1_HMNMYO_GCGCGGAGCG: gene migrated from ENSG00000179403 to ENSG00000179403 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy v2.0 | VWA1 | Gene migrated from ENSG00000179403 to ENSG00000179403 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy v1.176 | Bryony Thompson Copied gene VWA1 from panel Hereditary Neuropathy_CMT - isolated | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy v1.176 | VWA1 |
Bryony Thompson gene: VWA1 was added gene: VWA1 was added to Hereditary Neuropathy. Sources: Expert Review Green,Literature Mode of inheritance for gene: VWA1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: VWA1 were set to 33459760; 33693694; 33559681 Phenotypes for gene: VWA1 were set to Hereditary motor neuropathy |
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| Hereditary Neuropathy v1.119 | Bryony Thompson Copied STR VWA1_HMNMYO_GCGCGGAGCG from panel Hereditary Neuropathy_CMT - isolated | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Neuropathy v1.119 | VWA1_HMNMYO_GCGCGGAGCG |
Bryony Thompson STR: VWA1_HMNMYO_GCGCGGAGCG was added STR: VWA1_HMNMYO_GCGCGGAGCG was added to Hereditary Neuropathy. Sources: Literature,Expert Review Green,Expert Review Green,Literature paediatric-onset tags were added to STR: VWA1_HMNMYO_GCGCGGAGCG. Mode of inheritance for STR: VWA1_HMNMYO_GCGCGGAGCG was set to BIALLELIC, autosomal or pseudoautosomal Publications for STR: VWA1_HMNMYO_GCGCGGAGCG were set to 33559681; 33459760 Phenotypes for STR: VWA1_HMNMYO_GCGCGGAGCG were set to Neuropathy, hereditary motor, with myopathic features MIM#619216 |
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