ClinVar Miner

Submissions for variant NM_000519.3(HBD):c.39T>A (p.Asn13Lys)

gnomAD frequency: 0.00007  dbSNP: rs34313675
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
OMIM RCV000016199 SCV000036467 other HEMOGLOBIN A(2) NYU 2017-12-12 no assertion criteria provided literature only
OMIM RCV000016200 SCV000036468 other HEMOGLOBIN NYU 2017-12-12 no assertion criteria provided literature only

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