ClinVar Miner

Submissions for variant NM_000184.2(HBG2):c.68A>T (p.Asp23Val)

dbSNP: rs281864891
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000016125 SCV000036393 other HEMOGLOBIN F (GRANADA) 2016-08-18 no assertion criteria provided literature only

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