ClinVar Miner

Submissions for variant NM_003289.4(TPM2):c.703-9T>C

dbSNP: rs2131848760
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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 RCV001491218 SCV001695803 likely benign Arthrogryposis, distal, type 1A 2020-12-27 criteria provided, single submitter clinical testing

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