ClinVar Miner

Submissions for variant NM_024589.3(ROGDI):c.823-14C>T

dbSNP: rs201283169
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002097803 SCV002385411 likely benign Amelocerebrohypohidrotic syndrome 2024-04-17 criteria provided, single submitter clinical testing

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