Variants in gene DOCK6 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 13

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_020812.4(DOCK6):c.3752G>A (p.Arg1251Gln)	rs200390354	0.00245
NM_020812.4(DOCK6):c.4862T>C (p.Val1621Ala)	rs201738818	0.00166
NM_020812.4(DOCK6):c.5939+6C>T	rs200393834	0.00149
NM_020812.4(DOCK6):c.133G>A (p.Val45Ile)	rs183060698	0.00141
NM_020812.4(DOCK6):c.2594G>A (p.Arg865His)	rs199922090	0.00094
NM_020812.4(DOCK6):c.5582G>A (p.Arg1861His)	rs115035890	0.00093
NM_020812.4(DOCK6):c.518G>A (p.Arg173Gln)	rs373956807	0.00053
NM_020812.4(DOCK6):c.3895-7C>T	rs368322024	0.00026
NM_020812.4(DOCK6):c.5832+5G>A	rs181867999	0.00019
NM_020812.4(DOCK6):c.4350G>C (p.Leu1450=)	rs763073235	0.00002
NM_020812.4(DOCK6):c.172G>T (p.Asp58Tyr)
NM_020812.4(DOCK6):c.3163G>A (p.Val1055Met)	rs202209921
NM_020812.4(DOCK6):c.4204-3C>T

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.