Chromosome number :

1
2
3
4
5
6
7
8
9
X

chromosome
gene symbol
phenotype
20p13
?
Amyotrophic lateral sclerosis -ALS7
20p13-p12-3
?
Spinocerebellar ataxia 23 -SCA23
20q11-q13
?
Spinocerebellar ataxia, autosomal recessive 6 -SCAR6
20q13.12
JPH2
junctophilin-2
Hypertrophic cardiomyopathy with junctophilin defect -
Cardiomyopathy, familial hypertrophic, 17 -CMH17
20q13.31
MYLK2
myosin light chain kinase 2
cardiomyopathy, familial hypertrophic -CMH