ClinVar Miner

Submissions for variant NM_015271.5(TRIM2):c.1083G>T (p.Gly361=)

gnomAD frequency: 0.00003  dbSNP: rs779795369
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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 RCV000651811 SCV000773667 likely benign Charcot-Marie-Tooth disease type 2R 2024-01-04 criteria provided, single submitter clinical testing

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