ClinVar Miner

Submissions for variant NM_003289.4(TPM2):c.300C>T (p.Asp100=)

dbSNP: rs532190742
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000247592 SCV000309556 likely benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000247592 SCV000342991 benign not specified 2016-07-12 criteria provided, single submitter clinical testing
Invitae RCV000878219 SCV001021084 benign Arthrogryposis, distal, type 1A 2024-01-06 criteria provided, single submitter clinical testing
GeneDx RCV001711812 SCV001939813 benign not provided 2020-01-09 criteria provided, single submitter clinical testing

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