ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as benign

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NC_000011.10:g.5227540G>A rs10742584 0.96393
NC_000011.10:g.5227411G>A rs10742583 0.83082
NM_000518.5(HBB):c.9T>C (p.His3=) rs713040 0.82706
NC_000011.10:g.5227562T>G rs74049330 0.09404
NM_000518.5(HBB):c.-273T>C rs139703273 0.00604
NM_000518.5(HBB):c.93-23T>C rs111851677 0.00593
NM_000518.4(HBB):c.-133G>A rs72561473 0.00312
NM_000518.5(HBB):c.92+47T>G rs369341845 0.00040
NM_000518.4(HBB):c.-248A>G rs76306358 0.00031
NM_000518.5(HBB):c.246C>A (p.Leu82=) rs145669504 0.00022
NM_000518.5(HBB):c.294C>T (p.His98=) rs34515413 0.00022
NM_000518.5(HBB):c.-31C>T rs63750628 0.00003
NM_000518.5(HBB):c.50G>A (p.Gly17Asp) rs33962676 0.00003
NM_000518.4(HBB):c.263C>T (p.Thr88Ile) rs33993568 0.00002
NM_000518.5(HBB):c.170G>A (p.Gly57Asp) rs34439278 0.00002
NM_000518.5(HBB):c.262A>C (p.Thr88Pro) rs35553496 0.00002
NM_000518.4(HBB):c.68A>C (p.Glu23Ala) rs33936254 0.00001
NM_000518.4(HBB):c.-92C>G rs397515291
NM_000518.4(HBB):c.130G>C (p.Glu44Gln) rs33922842
NM_000518.4(HBB):c.157G>A (p.Asp53Asn) rs33961886
NM_000518.4(HBB):c.29C>G (p.Ser10Cys) rs33918131
NM_000518.5(HBB):c.-35A>G rs1847590703
NM_000518.5(HBB):c.40G>A (p.Ala14Thr) rs766266418
NM_000518.5(HBB):c.92+13G>T rs753444453

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