ClinVar Miner

List of variants in gene combination HBB, LOC107133510, LOC110006319 reported as uncertain significance for anemia (disease)

Included ClinVar conditions (263):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_000518.5(HBB):c.*53C>A rs886048393
NM_000518.5(HBB):c.*56A>T rs537944366
NM_000518.5(HBB):c.*91G>A rs193922549
NM_000518.5(HBB):c.316-30A>C rs193922558
NM_000518.5(HBB):c.316-70C>G rs193922560
NM_000518.5(HBB):c.353A>G (p.His118Arg) rs33935673

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