ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as likely benign for Dominant beta-thalassemia; Heinz body anemia; Hb SS disease; alpha Thalassemia; Malaria, susceptibility to; METHEMOGLOBINEMIA, BETA TYPE; Erythrocytosis, familial, 6; Hereditary persistence of fetal hemoglobin; Beta-thalassemia HBB/LCRB

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.-273T>C	rs139703273	0.00604
NM_000518.5(HBB):c.262A>C (p.Thr88Pro)	rs35553496	0.00002

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