Variants in gene MPI with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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_002435.3(MPI):c.303C>T (p.Leu101=)	rs139228075	0.00240
NM_002435.3(MPI):c.10C>T (p.Pro4Ser)	rs143982014	0.00133
NM_002435.3(MPI):c.678C>A (p.Ala226=)	rs199972529

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