Variants with conflicting interpretations "pathogenic" from Language and Genetics Department, Max Planck Institute for Psycholinguistics and "likely pathogenic" from any submitter

Minimum review status of the submission from Language and Genetics Department, Max Planck Institute for Psycholinguistics:		Collection method of the submission from Language and Genetics Department, Max Planck Institute for Psycholinguistics:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001349338.3(FOXP1):c.1540C>T (p.Arg514Cys)	rs869025203
NM_001349338.3(FOXP1):c.1541G>A (p.Arg514His)	rs797045586

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