ClinVar Miner

Submissions for variant NM_000518.5(HBB):c.346G>C (p.Ala116Pro)

dbSNP: rs34945623
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000016478 SCV000036746 other HEMOGLOBIN MADRID 2017-12-12 no assertion criteria provided literature only

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