List of variants in gene ZNF469 reported as benign by Eurofins NTD LLC (GA)

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: 24

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001367624.2(ZNF469):c.10990= (p.Ala3664=)	rs904783	0.99962
NM_001367624.2(ZNF469):c.8627A>G (p.His2876Arg)	rs1983014	0.99622
NM_001367624.2(ZNF469):c.3522G>A (p.Pro1174=)	rs9938800	0.89252
NM_001367624.2(ZNF469):c.4343C>T (p.Pro1448Leu)	rs4782300	0.87223
NM_001367624.2(ZNF469):c.4419T>G (p.Ser1473=)	rs12445417	0.85761
NM_001367624.2(ZNF469):c.1098A>C (p.Arg366Ser)	rs11640794	0.84448
NM_001367624.2(ZNF469):c.3568A>G (p.Lys1190Glu)	rs7197071	0.80067
NM_001367624.2(ZNF469):c.8604C>T (p.Arg2868=)	rs3812953	0.43642
NM_001367624.2(ZNF469):c.8093T>A (p.Leu2698Gln)	rs3812956	0.32763
NM_001367624.2(ZNF469):c.3516T>C (p.Arg1172=)	rs111557381	0.06017
NM_001367624.2(ZNF469):c.1285G>A (p.Ala429Thr)	rs113937803	0.04541
NM_001367624.2(ZNF469):c.1143C>A (p.Pro381=)	rs74032864	0.04134
NM_001367624.2(ZNF469):c.1827G>A (p.Ser609=)	rs148616993	0.02438
NM_001367624.2(ZNF469):c.10975G>A (p.Gly3659Arg)	rs3812951	0.02265
NM_001367624.2(ZNF469):c.1697C>T (p.Ala566Val)	rs181785233	0.00939
NM_001367624.2(ZNF469):c.2814G>A (p.Ala938=)	rs140480823	0.00931
NM_001367624.2(ZNF469):c.4421C>T (p.Ala1474Val)	rs199897247	0.00605
NM_001367624.2(ZNF469):c.9125G>A (p.Arg3042His)	rs150598363	0.00461
NM_001367624.2(ZNF469):c.10795G>T (p.Ala3599Ser)	rs199760004	0.00417
NM_001367624.2(ZNF469):c.7675A>G (p.Lys2559Glu)	rs146789160	0.00403
NM_001367624.2(ZNF469):c.8076G>A (p.Pro2692=)	rs149200506	0.00158
NM_001367624.2(ZNF469):c.946G>A (p.Glu316Lys)	rs368772806	0.00085
NM_001367624.2(ZNF469):c.10326G>C (p.Arg3442Ser)	rs56236932
NM_001367624.2(ZNF469):c.1069T>C (p.Ser357Pro)	rs11648572

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.