ClinVar Miner

List of variants in gene combination HBA1, HBA2, LOC106804612 reported as pathogenic for anemia (disease)

Included ClinVar conditions (258):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_000517.6(HBA2):c.410T>C (p.Leu137Pro) rs41469945

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