Variants in gene combination HBB, LOC106099062, LOC107133510 with conflicting interpretations reported as "other and "likely pathogenic"

Submission 1 (other) minimum review status:		Submission 1 (other) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_000518.4(HBB):c.208G>A (p.Gly70Ser)	rs33947415	0.00064
NM_000518.4(HBB):c.137T>C (p.Phe46Ser)	rs33978338
NM_000518.4(HBB):c.191A>G (p.His64Arg)	rs33985544
NM_000518.4(HBB):c.266T>C (p.Leu89Pro)	rs33940204
NM_000518.5(HBB):c.19GAG[1] (p.Glu8del)	rs63750928
NM_000518.5(HBB):c.200A>C (p.Lys67Thr)	rs35939489
NM_000518.5(HBB):c.205C>T (p.Leu69Phe)	rs33961459

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