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| Brugada syndrome v1.0 | TMEM168 | Gene migrated from ENSG00000146802 to ENSG00000146802 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.45 | Sangavi Sivagnanasundram Copied gene TMEM168 from panel Incidentalome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Brugada syndrome v0.45 | TMEM168 |
Sangavi Sivagnanasundram gene: TMEM168 was added gene: TMEM168 was added to Brugada syndrome. Sources: ClinGen Mode of inheritance for gene: TMEM168 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TMEM168 were set to https://search.clinicalgenome.org/CCID:009114 Phenotypes for gene: TMEM168 were set to Brugada syndrome MONDO:0015263 |
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