List of variants in gene DNM1L reported as likely pathogenic for Mitochondrial disease

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_012062.5(DNM1L):c.1088G>A (p.Gly363Asp)	rs2137520923
NM_012062.5(DNM1L):c.1201G>A (p.Gly401Ser)	rs1316999302
NM_012062.5(DNM1L):c.2128A>G (p.Arg710Gly)	rs2137612346
NM_012062.5(DNM1L):c.687_689dup (p.Leu230dup)	rs2137424964

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