List of variants in gene combination LOC130006551, TMEM126A reported as uncertain significance for inborn mitochondrial metabolism 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_032273.4(TMEM126A):c.-16G>C	rs548326357	0.00001
NM_032273.4(TMEM126A):c.-98C>G	rs2082473214

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