List of variants in gene DYNC2H1 reported as uncertain significance by Baylor Genetics

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001377.3(DYNC2H1):c.3682C>A (p.Leu1228Ile)	rs189806840	0.00189
NM_001377.3(DYNC2H1):c.5047C>T (p.Leu1683Phe)	rs201563576	0.00172
NM_001377.3(DYNC2H1):c.5798A>G (p.Glu1933Gly)	rs201829296	0.00076
NM_001377.3(DYNC2H1):c.5473A>G (p.Ile1825Val)	rs201860217	0.00029
NM_001377.3(DYNC2H1):c.11048C>T (p.Pro3683Leu)	rs1297881996	0.00001
NM_001377.3(DYNC2H1):c.12581C>T (p.Ser4194Phe)	rs886042136
NM_001377.3(DYNC2H1):c.4231T>C (p.Cys1411Arg)	rs1860951602
NM_001377.3(DYNC2H1):c.4360C>A (p.Leu1454Met)
NM_001377.3(DYNC2H1):c.61T>G (p.Phe21Val)	rs1858012761
NM_001377.3(DYNC2H1):c.970C>T (p.Leu324Phe)	rs1858493502

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