Variants with conflicting interpretations "likely pathogenic" from Fulgent Genetics, Fulgent Genetics and "other" from any submitter

Minimum review status of the submission from Fulgent Genetics, Fulgent Genetics:		Collection method of the submission from Fulgent Genetics, Fulgent Genetics:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_000518.4(HBB):c.208G>A (p.Gly70Ser)	rs33947415	0.00064
NM_000402.4(G6PD):c.185A>G (p.His62Arg)	rs137852340	0.00008
NM_000402.4(G6PD):c.583A>G (p.Asn195Asp)	rs137852331	0.00004
NM_000402.4(G6PD):c.233T>C (p.Ile78Thr)	rs76645461	0.00001
NM_000402.4(G6PD):c.1429G>A (p.Gly477Arg)	rs137852317
NM_000518.5(HBB):c.205C>T (p.Leu69Phe)	rs33961459

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