List of variants in gene DOCK7 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001367561.1(DOCK7):c.3935C>T (p.Thr1312Met)	rs59558623	0.00125
NM_001367561.1(DOCK7):c.2932C>T (p.Arg978Cys)	rs750049987	0.00021
NM_001367561.1(DOCK7):c.4480G>A (p.Val1494Ile)	rs746518826	0.00006
NM_001367561.1(DOCK7):c.4867A>G (p.Ile1623Val)	rs200800312	0.00006
NM_001367561.1(DOCK7):c.5080A>G (p.Met1694Val)	rs142608509	0.00005
NM_001367561.1(DOCK7):c.1531A>G (p.Ile511Val)	rs764347103	0.00001
NM_001367561.1(DOCK7):c.2503A>G (p.Asn835Asp)	rs747830413
NM_001367561.1(DOCK7):c.4192G>A (p.Glu1398Lys)	rs2149340289
NM_001367561.1(DOCK7):c.4688G>A (p.Ser1563Asn)
NM_001367561.1(DOCK7):c.5266G>A (p.Val1756Ile)
NM_001367561.1(DOCK7):c.5942A>G (p.Asn1981Ser)
NM_001367561.1(DOCK7):c.841A>G (p.Ile281Val)	rs1317549494
NM_001367561.1(DOCK7):c.847G>T (p.Ala283Ser)

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