Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 407975
Gene Symbol: MIR17HG
MIR17HG 		0.520 GeneticVariation disease BEFREE The deletion included MIR17HG, as expected by the FGLDS2 phenotype, and twelve genes from the keratoconus type 7 locus. 28159702 2017
Entrez Id: 407975
Gene Symbol: MIR17HG
MIR17HG 		0.520 Biomarker disease GENOMICS_ENGLAND A comparative genomic hybridization microarray was completed and a ∼3.6 Mb interstitial heterozygous deletion at 13q31.3 including MIR17HG was found consistent with Feingold syndrome-2. 26360630 2015
Entrez Id: 407975
Gene Symbol: MIR17HG
MIR17HG 		0.520 GeneticVariation disease BEFREE A comparative genomic hybridization microarray was completed and a ∼3.6 Mb interstitial heterozygous deletion at 13q31.3 including MIR17HG was found consistent with Feingold syndrome-2. 26360630 2015
Entrez Id: 407975
Gene Symbol: MIR17HG
MIR17HG 		0.520 ChromosomalRearrangement disease ORPHANET Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans. 21892160 2011
Entrez Id: 407975
Gene Symbol: MIR17HG
MIR17HG 		0.520 Biomarker disease GENOMICS_ENGLAND Germline deletion of the miR-17∼92 cluster causes skeletal and growth defects in humans. 21892160 2011
Entrez Id: 407975
Gene Symbol: MIR17HG
MIR17HG 		0.520 Biomarker disease GENOMICS_ENGLAND DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. 19344873 2009