ClinVar Miner

Submissions for variant NM_000587.4(C7):c.840T>G (p.Leu280=)

gnomAD frequency: 0.00001  dbSNP: rs766169920
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 RCV002094290 SCV002439880 likely benign not provided 2024-07-04 criteria provided, single submitter clinical testing

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