List of variants in gene DYNC1H1 reported as uncertain significance by University of Washington Center for Mendelian Genomics, University of Washington

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.10313G>A (p.Arg3438Gln)	rs1375729860	0.00001
NM_001376.5(DYNC1H1):c.10420C>T (p.Arg3474Trp)	rs757725348
NM_001376.5(DYNC1H1):c.10888G>A (p.Gly3630Ser)	rs2048578300
NM_001376.5(DYNC1H1):c.3161G>C (p.Trp1054Ser)	rs2048038170
NM_001376.5(DYNC1H1):c.4808G>C (p.Arg1603Thr)	rs1555409418
NM_001376.5(DYNC1H1):c.9954G>T (p.Lys3318Asn)	rs2048518511

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