ClinVar Miner

Submissions for variant NM_020461.4(TUBGCP6):c.3444G>A (p.Val1148=)

gnomAD frequency: 0.00007  dbSNP: rs1165628369
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002084707 SCV002324783 likely benign not provided 2023-01-12 criteria provided, single submitter clinical testing

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