List of variants in gene combination LOC101928335, MID2 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_012216.4(MID2):c.1656T>C (p.Asp552=)	rs150716868	0.00067
NM_012216.4(MID2):c.2144G>A (p.Arg715Gln)	rs370198556	0.00016
NM_012216.4(MID2):c.1662G>T (p.Leu554Phe)	rs749983502

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