List of variants in gene combination LOC126806368, MMADHC reported as uncertain significance for nutritional disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_015702.3(MMADHC):c.-16A>G	rs144111552	0.00009
NM_015702.3(MMADHC):c.-52-3C>G	rs886054922

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