chromosome	gene symbol	phenotype
6p23	ATXN1 ataxin 1	Spinocerebellar ataxia 1 -SCA1 Olivopontocerebellar atrophy I -OPCA1
6p23-p21	?	Spinocerebellar ataxia, autosomal recessive 3 -SCAR3
6p24	DSP desmoplakin	Arrhythmogenic right ventricular dysplasia, 8 -ARVD8
6q12-q16	?	Cardiomyopathy, dilated, 1K -CMD1K
6q14-q16	?	-
6q21	LAMA4 laminin alpha 4	Dilated cardiomyopathy due to laminin-alpha4 defect -LAMA4
6q21	FIG4 polyphosphoinositide phosphatase activity	charcot-marie-tooth disease, type 4j -CMT4J
6q21-q22	PEX7 peroxisomal biogenesis factor 7	Refsum disease, adult -RD
6q22-q23	LAMA2 laminin alpha 2 chain of merosin	Muscular dystrophy, congenital merosin-deficient -MDC1A
6q22.1	PLN phospholamban	Hypertrophic cardiomyopathy with phospholamban defect - Cardiomyopathy, familial hypertrophic, 18 -CMH18 Cardiomyopathy, dilated, 1P -CMD1P
6q23	?	Cardiomyopathy, dilated, 1F -CMD1F
6q23	?	Limb girdle muscular dystrophy 1E (autosomal dominant) -LGMD1E Cardiomyopathy, dilated, 1F -CMD1F
6q23-24	EYA4 eyes absent 4	Deafness, autosomal dominant nonsyndromic sensorineural 10 -DFNA10 Cardiomyopathy, dilated, 1J -CMD1J
6q23.3-q24.1	?	Spastic paraplegia 25 -SPG25
6q25	SYNE1 spectrin repeat containing, nuclear envelope 1 (nesprin 1)	Dilated cardiomyopathy with nesprin-1 defect - Spinocerebellar ataxia, autosomal recessive 8 -SCAR8 Emery-dreifuss muscular dystrophy 4 -EDMD4
6q27	TBP TATA box binding protein	Spinocerebellar ataxia 17 -SCA17