Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss. 25388789

2014
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Clinical characterization of a novel COCH mutation G87V in a Chinese DFNA9 family. 23993205

2013
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Whole exome sequencing identifies a novel DFNA9 mutation, C162Y. 22931125

2013
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT A novel COCH mutation associated with autosomal dominant nonsyndromic hearing loss disrupts the structural stability of the vWFA2 domain. 22610276

2012
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families. 18312449

2008
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Phenotype description of a novel DFNA9/COCH mutation, I109T. 17561763

2007
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9). 16835921

2006
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation BEFREE The study of clinical features of a DFNA9 family carrying a G88E COCH mutation and to compare this to the symptoms of those carrying a P51S/COCH mutation. 16151339

2005
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Mutations in COCH that result in non-syndromic autosomal dominant deafness (DFNA9) affect matrix deposition of cochlin. 12928864

2003
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease. 14512963

2003
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families. 11295836

2001
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene. 10400989

1999
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects. 9931344

1999
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
0.810 GeneticVariation UNIPROT Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction. 9806553

1998
dbSNP: rs121908928
rs121908928
COCH ; LOC100506071
A 0.810 CausalMutation CLINVAR