ClinVar Miner

Submissions for variant NM_006929.5(SKIC2):c.39T>C (p.Asp13=)

dbSNP: rs1253931216
Minimum review status: Collection method:
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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 RCV003557340 SCV004284177 likely benign not provided 2024-12-19 criteria provided, single submitter clinical testing

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