ZNF292, zinc finger protein 292, 23036

N. diseases: 53; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1925690
rs1925690
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0002395
Disease:
Alzheimer's Disease
0.800 GeneticVariation GWASCAT Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. 21116278 2011
dbSNP: rs1925690
rs1925690
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0002395
Disease:
Alzheimer's Disease
0.800 GeneticVariation GWASDB Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. 21116278 2011
dbSNP: rs9351120
rs9351120
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1135401779
rs1135401779
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C1843367
Disease:
Poor school performance
T 0.700 CausalMutation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C1837404
Disease:
High, narrow palate
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0920299
Disease:
Overriding toe
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0027092
Disease:
Myopia
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C1865598
Disease:
Alveolar ridge overgrowth
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C1859736
Disease:
Progressive spastic quadriplegia
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0158731
Disease:
Congenital pectus carinatum
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0007789
Disease:
Cerebral Palsy
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C4048268
Disease:
Cortical visual impairment
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0036572
Disease:
Seizures
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0263523
Disease:
Micronychia (disorder)
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0678230
Disease:
Congenital Epicanthus
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0426886
Disease:
Tapering fingers (finding)
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C1527366
Disease:
Salaam Seizures
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C1843367
Disease:
Poor school performance
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C4317146
Disease:
Acid reflux
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C1849367
Disease:
Nasal bridge wide
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0557874
Disease:
Global developmental delay
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C4551563
Disease:
Microcephaly (physical finding)
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0543888
Disease:
Epileptic encephalopathy
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C0013421
Disease:
Dystonia
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1554208945
rs1554208945
Entrez Id: 23036
Gene Symbol: ZNF292
ZNF292
CUI: C4020740
Disease:
Clinodactyly of the 4th toe
C 0.700 GeneticVariation CLINVAR