ClinVar Miner

Submissions for variant NM_003289.4(TPM2):c.773-10_773-9insCG

dbSNP: rs1554658504
Minimum review status: Collection method:
Minimum conflict level:
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 RCV001989409 SCV002282054 likely benign Arthrogryposis, distal, type 1A 2024-08-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004694102 SCV005195398 uncertain significance not provided criteria provided, single submitter not provided

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