ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.1664-24del

gnomAD frequency: 0.00297  dbSNP: rs534296796
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Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000409940 SCV000488479 likely benign Paragangliomas 5 2016-04-07 criteria provided, single submitter clinical testing

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