List of variants in gene DYNC1H1 reported as likely pathogenic by Labcorp Genetics (formerly Invitae), Labcorp

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.10030C>T (p.Arg3344Trp)	rs2048519381
NM_001376.5(DYNC1H1):c.10160T>C (p.Leu3387Pro)	rs1567019064
NM_001376.5(DYNC1H1):c.10574G>A (p.Arg3525His)	rs2152592202
NM_001376.5(DYNC1H1):c.11423GCA[2] (p.Ser3810del)
NM_001376.5(DYNC1H1):c.1777G>T (p.Val593Phe)	rs2047932647
NM_001376.5(DYNC1H1):c.1825A>G (p.Ile609Val)
NM_001376.5(DYNC1H1):c.2357G>A (p.Arg786His)
NM_001376.5(DYNC1H1):c.3015+17_3015+18delinsCT
NM_001376.5(DYNC1H1):c.4532C>T (p.Pro1511Leu)	rs1327664377
NM_001376.5(DYNC1H1):c.4699C>T (p.Arg1567Trp)	rs377013246
NM_001376.5(DYNC1H1):c.5885G>A (p.Arg1962His)	rs1057518287
NM_001376.5(DYNC1H1):c.9721A>G (p.Lys3241Glu)

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