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

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_002435.3(MPI):c.982C>T (p.Arg328Trp)	rs117089191	0.00577
NM_002435.3(MPI):c.303C>T (p.Leu101=)	rs139228075	0.00240
NM_002435.3(MPI):c.414G>A (p.Met138Ile)	rs150217523	0.00227
NM_002435.3(MPI):c.10C>T (p.Pro4Ser)	rs143982014	0.00133
NM_002435.3(MPI):c.1049C>T (p.Thr350Met)	rs116933453	0.00095
NM_002435.3(MPI):c.214A>C (p.Ser72Arg)	rs146699267	0.00031
NM_002435.3(MPI):c.1125G>A (p.Gly375=)	rs552854858	0.00016

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