List of variants in gene DYNC1H1 reported as uncertain significance by New York Genome Center

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001376.5(DYNC1H1):c.10522C>A (p.Leu3508Ile)	rs149496322	0.00019
NM_001376.5(DYNC1H1):c.3704A>G (p.Gln1235Arg)	rs867503066	0.00007
NM_001376.5(DYNC1H1):c.4884G>A (p.Arg1628=)	rs1273328322	0.00002
NM_001376.5(DYNC1H1):c.11684C>T (p.Thr3895Ile)	rs771563083	0.00001
NM_001376.5(DYNC1H1):c.13682C>T (p.Thr4561Met)	rs1376784009	0.00001
NM_001376.5(DYNC1H1):c.7262C>T (p.Thr2421Met)	rs770803375	0.00001
NM_001376.5(DYNC1H1):c.8275A>G (p.Ile2759Val)	rs1131691452	0.00001
NM_001376.5(DYNC1H1):c.11806G>A (p.Val3936Met)	rs780676515
NM_001376.5(DYNC1H1):c.1273G>T (p.Asp425Tyr)	rs2141272504
NM_001376.5(DYNC1H1):c.13855A>G (p.Ile4619Val)	rs879254286
NM_001376.5(DYNC1H1):c.5182G>A (p.Gly1728Ser)	rs77319596
NM_001376.5(DYNC1H1):c.568G>A (p.Glu190Lys)	rs1566996419
NM_001376.5(DYNC1H1):c.7438C>G (p.Pro2480Ala)	rs1018948570
NM_001376.5(DYNC1H1):c.83C>G (p.Ser28Trp)	rs765882472
NM_001376.5(DYNC1H1):c.8606G>T (p.Arg2869Leu)

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