ClinVar Miner

Submissions for variant NM_003289.4(TPM2):c.374+16G>C

dbSNP: rs769858878
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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 RCV002750381 SCV003017383 likely benign Arthrogryposis, distal, type 1A 2022-08-19 criteria provided, single submitter clinical testing

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