List of variants in gene MCM2 reported as uncertain significance for auditory system disease

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: 4

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HGVS	dbSNP
NM_004526.4(MCM2):c.1231G>A (p.Glu411Lys)
NM_004526.4(MCM2):c.1447C>T (p.Pro483Ser)
NM_004526.4(MCM2):c.1624C>T (p.Arg542Ter)	rs755835919
NM_004526.4(MCM2):c.277G>A (p.Glu93Lys)

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