List of variants in gene combination DNM1, LOC130002699 reported as benign for electroclinical syndrome

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004408.4(DNM1):c.2420C>G (p.Ser807Cys)	rs935756107	0.00022
NM_004408.4(DNM1):c.2467C>G (p.Pro823Ala)	rs2131299716
NM_004408.4(DNM1):c.2467C>T (p.Pro823Ser)	rs2131299716

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