Variants with conflicting interpretations "pathogenic" from SIB Swiss Institute of Bioinformatics and "uncertain significance" from any submitter

Minimum review status of the submission from SIB Swiss Institute of Bioinformatics:		Collection method of the submission from SIB Swiss Institute of Bioinformatics:
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_016034.5(MRPS2):c.413G>A (p.Arg138His)	rs758539748	0.00003
NM_005267.5(GJA8):c.263C>T (p.Pro88Leu)	rs782199122

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