ClinVar Miner

List of variants in gene combination HBB, LOC107133510, LOC110006319 reported as likely benign for not specified

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Gene type:
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Total variants: 18
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HGVS dbSNP
NM_000518.4(HBB):c.410G>A (p.Gly137Asp) rs33949486
NM_000518.4(HBB):c.430C>T (p.His144Tyr) rs33929415
NM_000518.5(HBB):c.*132+99T>C rs567259408
NM_000518.5(HBB):c.*96T>C rs34029390
NM_000518.5(HBB):c.316-125A>G rs63751175
NM_000518.5(HBB):c.316-146T>C rs35328027
NM_000518.5(HBB):c.316-184T>C rs193922557
NM_000518.5(HBB):c.316-238C>T rs558554234
NM_000518.5(HBB):c.316-28G>A rs771736852
NM_000518.5(HBB):c.316-37G>T rs193922559
NM_000518.5(HBB):c.316-45G>C rs140033163
NM_000518.5(HBB):c.316-70C>G rs193922560
NM_000518.5(HBB):c.324C>T (p.Gly108=) rs193922562
NM_000518.5(HBB):c.351T>C (p.His117=)
NM_000518.5(HBB):c.378A>T (p.Pro126=) rs1554917555
NM_000518.5(HBB):c.394C>A (p.Gln132Lys) rs33910209
NM_000518.5(HBB):c.397A>C (p.Lys133Gln) rs33953406
NM_000518.5(HBB):c.432C>T (p.His144=) rs36020563

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