ClinVar Miner

Submissions for variant NM_000349.3(STAR):c.466-11T>C

dbSNP: rs1053284504
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 RCV002111612 SCV002395183 likely benign not provided 2023-05-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005042726 SCV005680170 uncertain significance Congenital lipoid adrenal hyperplasia due to STAR deficency 2024-05-10 criteria provided, single submitter clinical testing

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