List of variants in gene combination HBB, LOC106099062, LOC107133510 reported as uncertain significance for Fetal hemoglobin quantitative trait locus 1

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000518.4(HBB):c.208G>A (p.Gly70Ser)	rs33947415	0.00064
NM_000518.5(HBB):c.246C>A (p.Leu82=)	rs145669504	0.00022
NM_000518.5(HBB):c.294C>T (p.His98=)	rs34515413	0.00022
NM_000518.4(HBB):c.34G>A (p.Val12Ile)	rs33974228	0.00007
NM_000518.5(HBB):c.85C>T (p.Leu29=)	rs33958088	0.00004
NM_000518.5(HBB):c.-31C>T	rs63750628	0.00003
NM_000518.5(HBB):c.274C>T (p.Leu92=)	rs769583496	0.00001

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