List of variants in gene MPI reported as benign for cardiovascular disorder

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: 20

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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.1053+31G>A	rs12593975	0.07316
NM_002435.3(MPI):c.*58C>T	rs2230479	0.06346
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.144+16T>A	rs138182675	0.00434
NM_002435.3(MPI):c.144+18T>A	rs186045258	0.00434
NM_002435.3(MPI):c.144+20T>A	rs190812626	0.00434
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
NM_002435.3(MPI):c.16+18dup
NM_002435.3(MPI):c.670+9A>G	rs7495739
NM_002435.3(MPI):c.678C>A (p.Ala226=)	rs199972529

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