List of variants in gene GFM2 reported as not provided for Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1; Combined oxidative phosphorylation deficiency 39

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_032380.5(GFM2):c.1984T>A (p.Ser662Thr)	rs141789665	0.00084
NM_032380.5(GFM2):c.569G>A (p.Arg190Gln)	rs761283105	0.00003
NM_032380.5(GFM2):c.1229T>A (p.Ile410Lys)	rs863224037	0.00001

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