List of variants in gene combination HBA2, LOC106804612 reported as likely benign for not specified

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000517.6(HBA2):c.375C>G (p.Ser125=)	rs775058691	0.00010
NM_000517.6(HBA2):c.95+36C>T	rs1455019991	0.00010
NM_000517.6(HBA2):c.*98T>C	rs1455865276	0.00007
NM_000517.6(HBA2):c.*103G>A	rs1363099908	0.00002
NM_000517.6(HBA2):c.414C>T (p.Thr138=)	rs371394396	0.00001
NM_000517.5(HBA2):c.-41C>G	rs1188584832
NM_000517.6(HBA2):c.148A>C (p.Ser50Arg)	rs1596569718
NM_000517.6(HBA2):c.271A>G (p.Lys91Glu)	rs63750093
NM_000517.6(HBA2):c.344C>T (p.Pro115Leu)	rs267607269

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