Gene: COCH ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121908930
rs121908930
COCH ; LOC100506071
0.010 GeneticVariation BEFREE A novel mutation (I109T) in COCH segregates with hearing impairment and vestibular dysfunction in the present family. 17561763

2007
dbSNP: rs28938175
rs28938175
COCH ; LOC100506071
0.010 GeneticVariation BEFREE Vestibular impairment starts earlier, progresses more rapidly, and, eventually, is more complete than hearing impairment in P51S COCH mutation carriers. 16151338

2005