ClinVar Miner

Submissions for variant NM_000518.4(HBB):c.86T>A (p.Leu29Gln)

dbSNP: rs33916412
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
OMIM RCV000016611 SCV000036880 other HEMOGLOBIN ST. LOUIS 2017-12-12 no assertion criteria provided literature only
OMIM RCV000016612 SCV000036881 pathogenic Heinz body anemia 1986-01-01 no assertion criteria provided literature only

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