List of variants in gene DOCK7 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001367561.1(DOCK7):c.4867A>G (p.Ile1623Val)	rs200800312	0.00006
NM_001367561.1(DOCK7):c.3743T>C (p.Ile1248Thr)	rs552981892	0.00001
NM_001367561.1(DOCK7):c.691C>G (p.Arg231Gly)	rs1254316274	0.00001

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