ClinVar Miner

Submissions for variant NM_003289.4(TPM2):c.241-5C>T

dbSNP: rs372898802
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001495374 SCV001700056 likely benign Arthrogryposis, distal, type 1A 2018-10-23 criteria provided, single submitter clinical testing

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