List of variants in gene MCM2 reported as uncertain significance for auditory system 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004526.4(MCM2):c.1510C>A (p.Pro504Thr)	rs150403449	0.00016
NM_004526.4(MCM2):c.2444G>A (p.Arg815His)	rs779228557	0.00003
NM_004526.4(MCM2):c.1447C>T (p.Pro483Ser)	rs767616299	0.00002
NM_004526.4(MCM2):c.850C>T (p.Arg284Cys)	rs766530339	0.00002
NM_004526.4(MCM2):c.1231G>A (p.Glu411Lys)	rs373695678	0.00001
NM_004526.4(MCM2):c.1624C>T (p.Arg542Ter)	rs755835919	0.00001
NM_004526.4(MCM2):c.1684C>T (p.Arg562Trp)	rs767499238
NM_004526.4(MCM2):c.277G>A (p.Glu93Lys)	rs199660068
NM_004526.4(MCM2):c.388C>T (p.Arg130Cys)	rs770528099
NM_004526.4(MCM2):c.758C>T (p.Ala253Val)

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