List of variants in gene MNX1 reported as pathogenic 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_005515.4(MNX1):c.53dup (p.Arg19fs)	rs1554594329
NM_005515.4(MNX1):c.752del (p.Gln251fs)	rs2134840169
NM_005515.4(MNX1):c.874C>T (p.Arg292Trp)	rs2134838763

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