List of variants in gene combination HBG2, LOC106099065 reported as pathogenic for hematologic disorder

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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: 10

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HGVS	dbSNP	gnomAD frequency
NC_000011.10:g.5254956A>G	rs63750654	0.00001
NC_000011.10:g.5254895G>A	rs34809449
NC_000011.10:g.5254895G>T	rs34809449
NC_000011.10:g.5254983G>C	rs35617911
NM_000184.2(HBG2):c.277C>T (p.His93Tyr)	rs35103459
NM_000184.3(HBG2):c.125T>C (p.Phe42Ser)	rs34878913
NM_000184.3(HBG2):c.190C>T (p.His64Tyr)	rs34474104
NM_000184.3(HBG2):c.191A>T (p.His64Leu)
NM_000184.3(HBG2):c.202G>A (p.Val68Met)	rs587776864
NM_000184.3(HBG2):c.85C>A (p.Leu29Met)	rs1278163109

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