List of variants in gene DNM1L reported as likely pathogenic for nutritional disorder

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_012062.5(DNM1L):c.28A>T (p.Lys10Ter)	rs745921568	0.00002

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