List of variants in gene combination HBG1, LOC106099064 reported as pathogenic for anemia

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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_000559.3(HBG1):c.-29G>A	rs368698783	0.15026
NM_000559.2(HBG1):c.-53-196C>T	rs35983258	0.00002
NM_000559.2(HBG1):c.-167C>T	rs281860601	0.00001
NC_000011.10:g.5250015G>A	rs1554921759
NM_000559.2(HBG1):c.-170G>A	rs35378915
NM_000559.2(HBG1):c.-53-195C>G	rs35321913
NM_000559.2(HBG1):c.-53-198T>C	rs35710727

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