ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.2073G>A (p.Gln691=)

gnomAD frequency: 0.00002  dbSNP: rs900830997
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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 RCV003824424 SCV004630403 likely benign not provided 2023-11-18 criteria provided, single submitter clinical testing

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