Variants with conflicting interpretations "likely pathogenic" from Rare Disease Center, Seoul National University Hospital and "pathogenic" from any submitter

Minimum review status of the submission from Rare Disease Center, Seoul National University Hospital:		Collection method of the submission from Rare Disease Center, Seoul National University Hospital:
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_003042.4(SLC6A1):c.131G>A (p.Arg44Gln)	rs794726859
NM_006772.3(SYNGAP1):c.1685C>T (p.Pro562Leu)	rs397514670

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