List of variants in gene combination HBB, LOC106099062, LOC107133510, LOC110006319 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_000518.5(HBB):c.315+1G>A	rs33945777	0.00003
NC_000011.10:g.5224303_5227790del
NC_000011.10:g.5225158_5227199del2042insCTTAT
NC_000011.10:g.5225895_5227411del1517insT
NC_000011.10:g.5226164_5227556del
NC_000011.10:g.5226452_5228055del
NM_000518.5(HBB):c.301_302delinsTCTGAGAACTT (p.Pro101delinsSerGluAsnPhe)	rs63750556
NM_000518.5(HBB):c.315+1G>C	rs33945777
NM_000518.5(HBB):c.315+1G>T	rs33945777
NM_000518.5(HBB):c.315+1del	rs63750774
NM_000518.5(HBB):c.315+2T>C	rs63750283
NM_000518.5(HBB):c.315+2T>G	rs63750283
NM_000518.5(HBB):c.315+2del	rs1564874813
NM_000518.5(HBB):c.315+4_315+5del	rs34750035
NM_000518.5(HBB):c.315+5G>C	rs35099082

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