List of variants in gene DNM1L reported as likely benign for peroxisomal disease

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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.741-19G>A	rs79520527	0.00897
NM_012062.5(DNM1L):c.1834A>T (p.Ile612Phe)	rs138133550	0.00073
NM_012062.5(DNM1L):c.1571T>C (p.Leu524Ser)	rs1031075173
NM_012062.5(DNM1L):c.1885-15del	rs863223951

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