ClinVar Miner

Submissions for variant NM_002024.6(FMR1):c.1622_1636del (p.Gln541_Gly545del)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Angen Gene Medicine Technology RCV003228810 SCV002605535 likely pathogenic Fragile X-associated tremor/ataxia syndrome 2022-11-22 no assertion criteria provided research

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