List of variants in gene MPI reported as benign by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_002435.3(MPI):c.1131A>G (p.Val377=)	rs1130741	0.45813
NM_002435.3(MPI):c.345+15G>A	rs11638130	0.35866
NM_002435.3(MPI):c.684C>T (p.Asn228=)	rs139190144	0.01985
NM_002435.3(MPI):c.345+16C>T	rs143242949	0.01224
NM_002435.3(MPI):c.762C>T (p.Ile254=)	rs12440159	0.00855
NM_002435.3(MPI):c.982C>T (p.Arg328Trp)	rs117089191	0.00577
NM_002435.3(MPI):c.1049C>T (p.Thr350Met)	rs116933453	0.00095
NM_002435.3(MPI):c.670+9A>G	rs7495739

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