ClinVar Miner

List of variants reported as uncertain significance for beta-thalassemia HBB/LCRB

Included ClinVar conditions (5):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_000518.4(HBB):c.208G>A (p.Gly70Ser) rs33947415
NM_000518.4(HBB):c.34G>A (p.Val12Ile) rs33974228
NM_000518.4(HBB):c.68A>C (p.Glu23Ala) rs33936254
NM_000518.5(HBB):c.*18C>A
NM_000518.5(HBB):c.*53C>A rs886048393
NM_000518.5(HBB):c.*56A>T rs537944366
NM_000518.5(HBB):c.*59A>G
NM_000518.5(HBB):c.*96T>C rs34029390
NM_000518.5(HBB):c.-133G>A rs72561473
NM_000518.5(HBB):c.-15C>A rs193922550
NM_000518.5(HBB):c.-25T>C rs886039874
NM_000518.5(HBB):c.-31C>T rs63750628
NM_000518.5(HBB):c.-75G>C rs63750400
NM_000518.5(HBB):c.-92C>G rs397515291
NM_000518.5(HBB):c.246C>A (p.Leu82=) rs145669504
NM_000518.5(HBB):c.274C>T (p.Leu92=) rs769583496
NM_000518.5(HBB):c.294C>T (p.His98=) rs34515413
NM_000518.5(HBB):c.316-369G>A rs1589891886
NM_000518.5(HBB):c.324C>T (p.Gly108=) rs193922562
NM_000518.5(HBB):c.402G>C (p.Val134=) rs113082294
NM_000518.5(HBB):c.85C>T (p.Leu29=)
NM_000518.5(HBB):c.93-23T>C rs111851677

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