ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as pathogenic for Heinz body anemia

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Total variants: 5
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HGVS dbSNP
NM_000518.4(HBB):c.127_129delTTT (p.Phe43del) rs41417446
NM_000518.4(HBB):c.86T>A (p.Leu29Gln) rs33916412
NM_000518.5(HBB):c.128T>C (p.Phe43Ser) rs34378160
NM_000518.5(HBB):c.295G>A (p.Val99Met) rs33933298
NM_000518.5(HBB):c.93G>T (p.Arg31Ser) rs1135071

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