List of variants reported as likely pathogenic for Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_024996.7(GFM1):c.689+908G>A	rs751069628	0.00011
NM_024996.7(GFM1):c.521A>G (p.Asn174Ser)	rs119470018	0.00002
NM_024996.7(GFM1):c.409G>A (p.Val137Met)	rs767325554	0.00001
NM_024996.7(GFM1):c.573-1G>C	rs2108009356

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