ZNF469 Chromosome 16

Zinc finger protein 469
571 variants 571 Health Risk

Upload your DNA to see your personal genotypes for variants in ZNF469.

What This Gene Does
This gene encodes a zinc-finger protein. Low-percent homology to certain collagens suggests that it may function as a transcription factor or extra-nuclear regulator factor for the synthesis or organization of collagen fibers. Mutations in this gene cause brittle cornea syndrome. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Zinc fingers C2H2-type
Locus Type
gene with protein product
Location
16q24.2
Ensembl
ENSG00000225614
Associated Conditions (8)
Cardiovascular phenotype
Ehlers-Danlos syndrome
Brittle cornea syndrome 1
ZNF469-related disorder
Brittle cornea syndrome
Keratoconus 1
Keratoconus
Connective tissue disorder
Key Variants
RS1002115521
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS1002770054
Conflicting classifications of pathogenicity
Ehlers-Danlos syndrome, Cardiovascular phenotype, Ehlers-Danlos syndrome
Health Risk
RS1003226456
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS1003677220
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS1004428835
Conflicting classifications of pathogenicity
Brittle cornea syndrome 1, Cardiovascular phenotype, Ehlers-Danlos syndrome
Health Risk
RS1006857833
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS1009769670
Conflicting classifications of pathogenicity
Ehlers-Danlos syndrome, Cardiovascular phenotype, Ehlers-Danlos syndrome
Health Risk
RS1010145375
Conflicting classifications of pathogenicity
Ehlers-Danlos syndrome, Cardiovascular phenotype, Ehlers-Danlos syndrome
Health Risk
RS1010183160
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS1011558573
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
RS1011775158
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Ehlers-Danlos syndrome, Cardiovascular phenotype
Health Risk
RS1015197481
Conflicting classifications of pathogenicity
Cardiovascular phenotype, Cardiovascular phenotype
Health Risk
All Variants (571)
RSID Category Clinical Significance Conditions
RS2507571255 Health Risk Pathogenic Cardiovascular phenotype, Cardiovascular phenotype
RS2507571459 Health Risk Pathogenic
RS2507571809 Health Risk Pathogenic
RS2507571828 Health Risk Pathogenic
RS2507572374 Health Risk Pathogenic
RS2507572620 Health Risk Pathogenic
RS2507572753 Health Risk Pathogenic
RS2507576747 Health Risk Pathogenic
RS2507576803 Health Risk Pathogenic
RS2507577344 Health Risk Pathogenic
RS2507577800 Health Risk Pathogenic
RS2507577853 Health Risk Pathogenic Cardiovascular phenotype, Cardiovascular phenotype
RS2507578316 Health Risk Pathogenic
RS2507578417 Health Risk Pathogenic
RS2507581312 Health Risk Pathogenic
RS2507581603 Health Risk Pathogenic
RS2507581694 Health Risk Pathogenic
RS2507582702 Health Risk Pathogenic
RS2507583248 Health Risk Pathogenic
RS2507583743 Health Risk Pathogenic
RS2507584642 Health Risk Pathogenic
RS2507585527 Health Risk Pathogenic
RS2507585886 Health Risk Pathogenic
RS2507586692 Health Risk Pathogenic
RS2507588285 Health Risk Pathogenic
RS2507588380 Health Risk Pathogenic
RS2507588444 Health Risk Pathogenic
RS2507588914 Health Risk Pathogenic Cardiovascular phenotype, Cardiovascular phenotype
RS2507589187 Health Risk Pathogenic
RS2507589689 Health Risk Pathogenic
RS2507589736 Health Risk Pathogenic
RS2507590369 Health Risk Pathogenic
RS2507590620 Health Risk Pathogenic
RS2507592045 Health Risk Pathogenic
RS2507592471 Health Risk Pathogenic
RS2507594138 Health Risk Pathogenic
RS2507594334 Health Risk Pathogenic
RS2507594973 Health Risk Pathogenic
RS2507595241 Health Risk Pathogenic
RS2507596154 Health Risk Pathogenic
RS2507596437 Health Risk Pathogenic
RS2507597158 Health Risk Pathogenic
RS2507598029 Health Risk Pathogenic
RS2507598165 Health Risk Pathogenic
RS2507598343 Health Risk Pathogenic
RS2507599497 Health Risk Pathogenic
RS2507600316 Health Risk Pathogenic
RS2507601279 Health Risk Pathogenic
RS2507602020 Health Risk Pathogenic
RS2507602463 Health Risk Pathogenic
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