ClinVar Miner

List of variants in gene combination HBB, HBD, LOC106099062, LOC106099063, LOC107133510, LOC110006319 reported as pathogenic for Anemia; Abnormal hemoglobin; Persistence of hemoglobin F; Reduced beta/alpha synthesis ratio

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NC_000011.10:g.5226570_5233984del

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