Variants with conflicting interpretations "uncertain significance" from Revvity Omics, Revvity and "likely risk allele" from any submitter

Minimum review status of the submission from Revvity Omics, Revvity:		Collection method of the submission from Revvity Omics, Revvity:
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_005419.4(STAT2):c.250C>A (p.Gln84Lys)	rs150901100	0.00024
NM_005419.4(STAT2):c.1466C>T (p.Pro489Leu)	rs138681270

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