Variants in gene MTOR with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004958.4(MTOR):c.5663T>G (p.Phe1888Cys)	rs869312666
NM_004958.4(MTOR):c.7216G>A (p.Val2406Met)	rs1557739557

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