ClinVar Miner

Submissions for variant NM_000558.3(HBA1):c.272A>T (p.Lys91Met)

dbSNP: rs33911106
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 RCV000017044 SCV000037316 other HEMOGLOBIN HANDA 2016-07-20 no assertion criteria provided literature only
OMIM RCV000017045 SCV000037317 other HEMOGLOBIN MUNAKATA 2016-07-20 no assertion criteria provided literature only

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