List of variants in gene combination HBA2, LOC106804612 reported as benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000517.6(HBA2):c.-24C>G	rs772829778	0.06872
NM_000517.6(HBA2):c.300+55T>G	rs2362746	0.01848
NM_000517.6(HBA2):c.237C>A (p.Asn79Lys)	rs281860607
NM_000517.6(HBA2):c.237C>G (p.Asn79Lys)	rs281860607
NM_000517.6(HBA2):c.301-24delinsCTCGGCCC	rs1596570272
NM_000517.6(HBA2):c.95+39C>T	rs1025977498

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