ClinVar Miner

Submissions for variant NM_003002.4(SDHD):c.6G>A (p.Ala2=) (rs1592777160)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000945164 SCV001091154 likely benign not provided 2018-08-31 criteria provided, single submitter clinical testing
Invitae RCV001446216 SCV001649259 likely benign Carney-Stratakis syndrome; Pheochromocytoma; Paragangliomas 1; Cowden syndrome 3 2018-08-27 criteria provided, single submitter clinical testing

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