ClinVar Miner

Submissions for variant NM_000782.5(CYP24A1):c.733-9T>C

gnomAD frequency: 0.00009  dbSNP: rs895309596
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000971690 SCV001119349 likely benign not provided 2023-10-11 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002503076 SCV002805663 likely benign Hypercalcemia, infantile, 1 2021-10-27 criteria provided, single submitter clinical testing

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