Variants in gene PTS with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
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_000317.3(PTS):c.315-3T>C	rs189365250	0.00436
NM_000317.3(PTS):c.372A>T (p.Val124=)	rs139969809	0.00011
NM_000317.3(PTS):c.132C>T (p.Asn44=)	rs763556416	0.00006

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