List of variants in gene combination HBB, LOC107133510, LOC110006319 reported as 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.315+16G>C	rs10768683	0.82893
NM_000518.5(HBB):c.316-185C>T	rs1609812	0.82712
NM_000518.4(HBB):c.*316A>C	rs7110263	0.81846
NM_000518.4(HBB):c.*233G>C	rs12788013	0.10429
NM_000518.4(HBB):c.*182G>A	rs113969885	0.01596
NM_000518.4(HBB):c.*353G>A	rs112988270	0.00595
NM_000518.5(HBB):c.316-37G>T	rs193922559	0.00058
NM_000518.4(HBB):c.*138T>G	rs560643693	0.00056
NM_000518.5(HBB):c.316-125A>G	rs63751175	0.00045
NM_000518.5(HBB):c.316-45G>C	rs140033163	0.00024
NM_000518.5(HBB):c.315+70G>C	rs373152208	0.00021
NM_000518.4(HBB):c.410G>A (p.Gly137Asp)	rs33949486	0.00001
NM_000518.4(HBB):c.430C>T (p.His144Tyr)	rs33929415	0.00001

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