List of variants in gene MMADHC reported as uncertain significance by GeneDx

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_015702.3(MMADHC):c.646C>G (p.Arg216Gly)	rs141093638	0.00181
NM_015702.3(MMADHC):c.41A>G (p.Tyr14Cys)	rs756550492	0.00001
NM_015702.3(MMADHC):c.742C>T (p.Arg248Cys)	rs544727246	0.00001

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