RS199473690 DNMT1
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What This Variant Does
"CLNSIG=255
Associated Conditions
Hereditary sensory neuropathy-deafness-dementia syndrome
Charcot-Marie-Tooth disease
Autosomal dominant cerebellar ataxia
deafness and narcolepsy
Hereditary sensory neuropathy-deafness-dementia syndrome
Charcot-Marie-Tooth disease
Autosomal dominant cerebellar ataxia
deafness and narcolepsy
Other Variants in DNMT1