ClinVar Miner

Submissions for variant NM_003000.3(SDHB):c.234G>A (p.Lys78=)

dbSNP: rs776971836
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001458553 SCV001662376 likely benign Gastrointestinal stromal tumor; Paragangliomas 4; Pheochromocytoma 2022-12-24 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003320838 SCV004024746 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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