List of variants in gene combination HBA1, HBA2, LOC106804612 reported as other

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000517.4(HBA2):c.427T>C (p.Ter143Gln)	rs41464951	0.00006
NM_000517.6(HBA2):c.122A>T (p.Lys41Met)	rs281864828
NM_000517.6(HBA2):c.150C>A (p.Ser50Arg)	rs41518249
NM_000517.6(HBA2):c.294C>A (p.Asn98Lys)	rs41338947
NM_000517.6(HBA2):c.369C>G (p.His123Gln)	rs41479347
NM_000517.6:c.63C>A
NM_000558.5(HBA1):c.132C>G (p.Phe44Leu)
NM_000558.5(HBA1):c.219C>A (p.His73Gln)

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