List of variants in gene MCAT reported as pathogenic for optic atrophy

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_173467.5(MCAT):c.424-2A>G
NM_173467.5(MCAT):c.823G>A (p.Glu275Lys)
NM_173467.5(MCAT):c.[242T>G;634C>T]

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