ClinVar Miner

List of variants in gene combination HBA2, LOC106804612 reported as not provided for alpha Thalassemia

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Total variants: 6
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HGVS dbSNP gnomAD frequency
NM_000517.6(HBA2):c.*94A>G rs63751269
NM_000517.6(HBA2):c.207C>G (p.Asn69Lys) rs111033601
NM_000517.6(HBA2):c.2T>C (p.Met1Thr) rs111033603
NM_000517.6(HBA2):c.377T>C (p.Leu126Pro) rs41397847
NM_000517.6(HBA2):c.94_95del (p.Arg32fs) rs1057519637
NM_000517.6(HBA2):c.95+2_95+6del rs41474145

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