List of variants in gene MCM5 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_006739.4(MCM5):c.772G>A (p.Val258Ile)	rs2230933	0.00443
NM_006739.4(MCM5):c.335G>A (p.Arg112Gln)	rs112123125	0.00242
NM_006739.4(MCM5):c.1893C>T (p.Phe631=)	rs545458717	0.00009

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