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1 Pancreatic agenesis

X-ray sensitivity Spinocerebellar ataxia

Chorea, hereditary benign

Osteosarcoma Bladder cancer Wilson disease

Meniere disease Glycogen storage disease

Alzheimer's disease Machado-Joseph disease

Oligodontia

DNA mismatch repair gene MLH3 Diabetes mellitus, insulin-dependent

Hair color, brown

Prader-Wllll/Angelman syndrome (paternally Imprinted) Eye color, brown

Albinism, oculocutaneous, type II and ocular

Muscular dystrophy, limb-girdle, type 2A Dyslexia

114 million bases

Eye color, green/blue

Alzheimer disease, late onset

Maple syrup urine disease, type Ia

Hirschsprung disease

67 million bases

Marfan syndrome

Tay-Sachs disease

Hypercholesterolemia, familial, autosomal recessive

109 million bases

106 million bases

Insomnia, fatal familial

Low density lipoprotein Gigantism receptor

Severe combined Colon cancer immunodeficiency disease DNA ligase I deficiency Hair color, brown

Alzheimer's disease, APP-related Amytrophic lateral sclerosis

Down syndrome (critical region)

Breast cancer Prion protein

72 million bases

50 million bases

CxiO

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