ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as likely benign for not specified

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Total variants: 16
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HGVS dbSNP
NM_000518.4(HBB):c.23A>G (p.Glu8Gly) rs34387455
NM_000518.4(HBB):c.263C>A (p.Thr88Lys) rs33993568
NM_000518.4(HBB):c.29C>G (p.Ser10Cys) rs33918131
NM_000518.5(HBB):c.174C>T (p.Asn58=) rs35278874
NM_000518.5(HBB):c.180G>A (p.Lys60=) rs34621955
NM_000518.5(HBB):c.207C>T (p.Leu69=) rs112287010
NM_000518.5(HBB):c.246C>A (p.Leu82=) rs145669504
NM_000518.5(HBB):c.262A>C (p.Thr88Pro) rs35553496
NM_000518.5(HBB):c.286A>G (p.Lys96Glu) rs33914359
NM_000518.5(HBB):c.288G>A (p.Lys96=) rs36038739
NM_000518.5(HBB):c.294C>T (p.His98=) rs34515413
NM_000518.5(HBB):c.31G>A (p.Ala11Thr) rs63750717
NM_000518.5(HBB):c.33C>T (p.Ala11=) rs35799536
NM_000518.5(HBB):c.45G>A (p.Leu15=) rs762782573
NM_000518.5(HBB):c.84C>T (p.Ala28=) rs748296717
NM_000518.5(HBB):c.93-15T>C rs35456885

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