List of variants in gene DYNC2H1 reported as likely benign by Genetic Services Laboratory, University of Chicago

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_001377.3(DYNC2H1):c.10864C>A (p.Arg3622=)	rs117178504	0.00672
NM_001377.3(DYNC2H1):c.1263C>A (p.Phe421Leu)	rs142881106	0.00365
NM_001377.3(DYNC2H1):c.6909C>T (p.Tyr2303=)	rs191012679	0.00210
NM_001377.3(DYNC2H1):c.7128A>G (p.Ala2376=)	rs371410128	0.00193
NM_001377.3(DYNC2H1):c.3682C>A (p.Leu1228Ile)	rs189806840	0.00189
NM_001377.3(DYNC2H1):c.12366+8A>G	rs200404815	0.00156
NM_001377.3(DYNC2H1):c.6918A>G (p.Ser2306=)	rs368824340	0.00102
NM_001377.3(DYNC2H1):c.3744+9C>T	rs142483417	0.00101
NM_001377.3(DYNC2H1):c.2244C>T (p.His748=)	rs373707570	0.00039
NM_001377.3(DYNC2H1):c.8946+10A>C	rs550521675	0.00001
NM_001377.3(DYNC2H1):c.11096-9A>G
NM_001377.3(DYNC2H1):c.5784A>G (p.Gly1928=)	rs1555057066

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