ClinVar Miner

Submissions for variant NM_000518.4(HBB):c.182T>A (p.Val61Glu)

dbSNP: rs33931779
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000016666 SCV000036936 pathogenic Beta-plus-thalassemia 1991-01-15 no assertion criteria provided literature only
OMIM RCV000016667 SCV000036937 other HEMOGLOBIN CAGLIARI 2017-12-12 no assertion criteria provided literature only

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