List of variants in gene DOCK7 reported as likely pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001367561.1(DOCK7):c.1872-6A>T	rs756259590	0.00033
NM_001367561.1(DOCK7):c.1801-1593_1801-1590del	rs1571649028
NM_001367561.1(DOCK7):c.1872-6del	rs1161370391
NM_001367561.1(DOCK7):c.5634+1G>A	rs1646006817

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