ClinVar Miner

Submissions for variant NM_021814.5(ELOVL5):c.622-12C>T

gnomAD frequency: 0.00449  dbSNP: rs115953222
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV002034842 SCV002107311 likely benign not provided 2021-05-17 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002034842 SCV003030939 benign not provided 2025-01-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002034842 SCV005222038 likely benign not provided criteria provided, single submitter not provided

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