List of variants in gene DOK7 reported as uncertain significance for not specified

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_173660.5(DOK7):c.973C>T (p.Arg325Trp)	rs376280466	0.00006
NM_173660.5(DOK7):c.1451C>T (p.Pro484Leu)	rs1057518522	0.00003
NM_173660.5(DOK7):c.638G>A (p.Arg213Gln)	rs371408752	0.00003
NM_173660.5(DOK7):c.635T>C (p.Leu212Pro)	rs553985062	0.00001
NM_173660.4:c.(?_2670)_(14056_?)del
NM_173660.5(DOK7):c.1501A>C (p.Asn501His)
NM_173660.5(DOK7):c.212A>T (p.Tyr71Phe)	rs771583740
NM_173660.5(DOK7):c.512G>A (p.Gly171Asp)	rs1286619522

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