Variants with conflicting interpretations "likely benign" from SingHealth Duke-NUS Institute of Precision Medicine and "benign" from any submitter

Minimum review status of the submission from SingHealth Duke-NUS Institute of Precision Medicine:		Collection method of the submission from SingHealth Duke-NUS Institute of Precision Medicine:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000277.3(PAH):c.158G>A (p.Arg53His)	rs118092776	0.00091
NM_000436.4(OXCT1):c.173C>T (p.Thr58Met)	rs75134564	0.00053
NM_001875.5(CPS1):c.-4_-3insTTC	rs61509952

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