ClinVar Miner

Submissions for variant NM_205861.3(DHDDS):c.324-4T>G

gnomAD frequency: 0.00001  dbSNP: rs747118618
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 RCV001313825 SCV001504332 likely benign Retinitis pigmentosa 59 2024-02-09 criteria provided, single submitter clinical testing
Natera, Inc. RCV001313825 SCV002085955 uncertain significance Retinitis pigmentosa 59 2020-10-29 no assertion criteria provided clinical testing

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