ClinVar Miner

List of variants in gene DNM1L reported as uncertain significance for See cases

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_012062.5(DNM1L):c.2151A>G (p.Leu717=)	rs149256584	0.00016
NM_012062.5(DNM1L):c.285C>T (p.His95=)	rs374173514	0.00015

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