List of variants in gene DYNC1H1 reported as uncertain significance for bone 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.8200G>A (p.Val2734Met)	rs376679623	0.00011
NM_001376.5(DYNC1H1):c.4030G>A (p.Asp1344Asn)	rs575285403	0.00001
NM_001376.5(DYNC1H1):c.12628T>C (p.Ser4210Pro)	rs2503865787

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