ClinVar Miner

Submissions for variant NM_198994.3(TGM6):c.1668G>T (p.Gly556=)

gnomAD frequency: 0.00007  dbSNP: rs781154109
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001644783 SCV000844471 benign not specified 2021-03-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003558539 SCV004284651 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing

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