ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as benign by Department of Medical Genetics, Yunnan Provincial Key Laboratory for Birth Defects and Genetic Diseases, The First People’s Hospital of Yunnan Province

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_000518.5(HBB):c.40G>A (p.Ala14Thr) rs766266418

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