List of variants in gene ZNF469 reported as benign by Illumina Laboratory Services, Illumina

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: 25

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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.1529G>C (p.Gly510Ala)	rs7199961	0.99603
NM_001367624.2(ZNF469):c.11856C>T (p.Ser3952=)	rs4782362	0.98833
NM_001367624.2(ZNF469):c.*788G>A	rs3894713	0.98791
NM_001367624.2(ZNF469):c.5661C>G (p.Thr1887=)	rs9931465	0.89293
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.1776A>G (p.Pro592=)	rs12927001	0.86712
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.*1001A>G	rs3848234	0.80892
NM_001367624.2(ZNF469):c.3568A>G (p.Lys1190Glu)	rs7197071	0.80067
NM_001367624.2(ZNF469):c.11757A>G (p.Pro3919=)	rs4782301	0.77860
NM_001367624.2(ZNF469):c.2130T>C (p.Pro710=)	rs12918876	0.60216
NM_001367624.2(ZNF469):c.10972G>C (p.Glu3658Gln)	rs1105066	0.44478
NM_001367624.2(ZNF469):c.8604C>T (p.Arg2868=)	rs3812953	0.43642
NM_001367624.2(ZNF469):c.7156G>C (p.Gly2386Arg)	rs12598474	0.36151
NM_001367624.2(ZNF469):c.8093T>A (p.Leu2698Gln)	rs3812956	0.32763
NM_001367624.2(ZNF469):c.*8G>A	rs45504291	0.24166
NM_001367624.2(ZNF469):c.6462G>A (p.Pro2154=)	rs61472141	0.10977
NM_001367624.2(ZNF469):c.*551TCCTCCCTCTGACCACAGGGTCATGCC[3]	rs6145934
NM_001367624.2(ZNF469):c.*618T>G	rs3859020
NM_001367624.2(ZNF469):c.*870del	rs35684712
NM_001367624.2(ZNF469):c.1069T>C (p.Ser357Pro)	rs11648572

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