ClinVar Miner

List of variants in gene DYNC2LI1 reported as uncertain significance by Revvity Omics, Revvity

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_016008.4(DYNC2LI1):c.326T>A (p.Phe109Tyr)	rs535890611	0.00001
NM_016008.4(DYNC2LI1):c.930C>A (p.Asp310Glu)	rs2467093294

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