ClinVar Miner

Submissions for variant NM_001953.5(TYMP):c.194G>A (p.Ser65Asn)

dbSNP: rs570047465
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000944682 SCV001090660 benign not provided 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV000944682 SCV001795225 likely benign not provided 2021-01-06 criteria provided, single submitter clinical testing
Natera, Inc. RCV001276281 SCV001462375 benign Mitochondrial neurogastrointestinal encephalomyopathy 2020-09-16 no assertion criteria provided clinical testing

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