ClinVar Miner

Submissions for variant NM_000548.5(TSC2):c.4223G>A (p.Gly1408Asp)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genesolutions, Medical Genetics Institutes, Ho Chi Minh City, Vietnam RCV003234985 SCV003934957 pathogenic Tuberous sclerosis 2 2022-06-22 criteria provided, single submitter clinical testing

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