List of variants in gene LYRM7 reported as uncertain significance for Mitochondrial complex III deficiency nuclear type 8

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_181705.4(LYRM7):c.264C>A (p.Asp88Glu)	rs199579347	0.00005
NM_181705.4(LYRM7):c.120C>A (p.Phe40Leu)	rs2149661849
NM_181705.4(LYRM7):c.128A>G (p.Asn43Ser)
NM_181705.4(LYRM7):c.142TCT[1] (p.Ser49del)
NM_181705.4(LYRM7):c.244+6T>G	rs1755807014

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