ClinVar Miner

Submissions for variant NM_152594.3(SPRED1):c.1194C>T (p.Asp398=)

dbSNP: rs2141016629
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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
Invitae RCV001421514 SCV001624039 likely benign Legius syndrome 2022-08-06 criteria provided, single submitter clinical testing

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