Variants with conflicting interpretations "uncertain significance" from SingHealth Duke-NUS Institute of Precision Medicine and "likely pathogenic" from Fulgent Genetics, Fulgent Genetics

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001370658.1(BTD):c.1270G>C (p.Asp424His)	rs13078881	0.03225

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