ClinVar Miner

List of variants in gene DYNC1H1 reported as uncertain significance by Institute of Human Genetics, University Hospital Muenster

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_001376.5(DYNC1H1):c.5411G>A (p.Arg1804Gln)	rs746543001	0.00001
NM_001376.5(DYNC1H1):c.12166G>A (p.Glu4056Lys)	rs2152596506

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