ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.316-292del

dbSNP: rs1170203019
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
Invitae RCV000941648 SCV001087541 likely benign not provided 2023-12-23 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000941648 SCV001134228 likely benign not provided 2023-09-01 criteria provided, single submitter clinical testing

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