ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.316C>T (p.Leu106Phe)

dbSNP: rs34022507
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000506082 SCV000601286 uncertain significance not specified 2017-02-15 criteria provided, single submitter clinical testing
OMIM RCV000016738 SCV000037008 other HEMOGLOBIN SOUTH MILWAUKEE 2017-12-12 no assertion criteria provided literature only

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