ClinVar Miner

List of variants in gene combination HBB, LOC106099062, LOC107133510 reported by Unidade de Eritropatologia e Metabolismo do Ferro, Centro Hospitalar e Universitário de Coimbra

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000518.4(HBB):c.110C>A (p.Pro37His)	rs33993004
NM_000518.5(HBB):c.300T>A (p.Asp100Glu)	rs34013622

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