ClinVar Miner

Submissions for variant NM_001953.5(TYMP):c.418-7C>T

dbSNP: rs2069479747
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002069440 SCV002472525 likely benign not provided 2024-07-10 criteria provided, single submitter clinical testing
Natera, Inc. RCV001278862 SCV001465908 uncertain significance Mitochondrial neurogastrointestinal encephalomyopathy 2020-08-14 no assertion criteria provided clinical testing

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