List of variants in gene MCM7 reported as pathogenic for autosomal recessive disease

Minimum submission review status:		Collection method:
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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	gnomAD frequency
NM_005916.5(MCM7):c.1616A>G (p.Tyr539Cys)	rs778583017	0.00001
NM_005916.5(MCM7):c.1579C>T (p.Arg527Ter)	rs76705400
NM_005916.5(MCM7):c.415C>T (p.Gln139Ter)	rs1054083917
NM_005916.5(MCM7):c.776G>C (p.Gly259Ala)	rs758105856

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