ClinVar Miner

Submissions for variant NM_006509.4(RELB):c.615C>T (p.Asp205=)

gnomAD frequency: 0.00081  dbSNP: rs372256791
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 RCV001469265 SCV001673343 likely benign not provided 2025-01-13 criteria provided, single submitter clinical testing

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