ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.4698G>A (p.Leu1566=)

gnomAD frequency: 0.00001  dbSNP: rs376881715
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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 RCV002189560 SCV002349902 likely benign not provided 2022-09-27 criteria provided, single submitter clinical testing

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