ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as not provided for Beta-thalassemia, dominant inclusion body type; Fetal hemoglobin quantitative trait locus 1; Hb SS disease; beta Thalassemia

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Total variants: 1
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HGVS dbSNP
NM_000518.4(HBB):c.208G>A (p.Gly70Ser) rs33947415

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