Variants with conflicting interpretations "likely benign" from ClinGen PAH Variant Curation Expert Panel and "benign" from any submitter

Minimum review status of the submission from ClinGen PAH Variant Curation Expert Panel:		Collection method of the submission from ClinGen PAH Variant Curation Expert Panel:
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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000277.3(PAH):c.820A>G (p.Lys274Glu)	rs142934616	0.00496
NM_000277.3(PAH):c.772C>T (p.Leu258=)	rs75065106	0.00272
NM_000277.3(PAH):c.706+17G>T	rs62508592	0.00087
NM_000277.3(PAH):c.837C>T (p.Pro279=)	rs138355741	0.00008

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