ClinVar Miner

Submissions for variant NM_003002.4(SDHD):c.99A>G (p.Ala33=)

dbSNP: rs2135267182
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002240445 SCV001674069 likely benign Carney-Stratakis syndrome; Pheochromocytoma; Paragangliomas with sensorineural hearing loss; Cowden syndrome 3 2020-02-27 criteria provided, single submitter clinical testing

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