List of variants in gene DYNC1H1 reported as uncertain significance for Autism spectrum 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.10195C>T (p.Gln3399Ter)
NM_001376.5(DYNC1H1):c.12419G>A (p.Arg4140His)	rs770451110
NM_001376.5(DYNC1H1):c.12653C>T (p.Thr4218Met)

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