List of variants in gene combination HBD, LOC106099063 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000519.4(HBD):c.225C>T (p.Gly75=)	rs113727122	0.00024
NM_000519.4(HBD):c.83C>A (p.Ala28Asp)	rs751533248	0.00004
NM_000519.4(HBD):c.97C>T (p.Leu33=)	rs746437742	0.00001
NM_000519.4(HBD):c.76G>A (p.Gly26Ser)	rs886048395

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