Variants with conflicting interpretations "likely pathogenic" from Baylor Genetics and "affects" from any submitter

Minimum review status of the submission from Baylor Genetics:		Collection method of the submission from Baylor 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_000441.2(SLC26A4):c.1667A>G (p.Tyr556Cys)	rs763006761	0.00002
NM_000441.2(SLC26A4):c.2007C>A (p.Asp669Glu)	rs749013429	0.00001
NM_000441.2(SLC26A4):c.2048T>C (p.Phe683Ser)	rs1060499808	0.00001
NM_000441.2(SLC26A4):c.269C>T (p.Ser90Leu)	rs370588279
NM_000441.2(SLC26A4):c.367C>T (p.Pro123Ser)	rs984967571
NM_000441.2(SLC26A4):c.416G>C (p.Gly139Ala)	rs756272252

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