ClinVar Miner

Submissions for variant NM_145698.5(ACBD5):c.376-68del

dbSNP: rs59068315
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
GeneDx RCV001596840 SCV001832220 benign not provided 2021-05-08 criteria provided, single submitter clinical testing

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