RS781301028 DNMT1

Health Risk Chr 19:10137091
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Associated Conditions
Hereditary sensory neuropathy-deafness-dementia syndrome
Autosomal dominant cerebellar ataxia
deafness and narcolepsy
Hereditary sensory neuropathy-deafness-dementia syndrome
Autosomal dominant cerebellar ataxia
deafness and narcolepsy
Other Variants in DNMT1
rs199473690 rs199473691 rs397509391 rs397509392 rs397509393 rs199473692 rs146112081 rs141856197 rs148831705 rs138841970
Ask Dr. Hemsworth about this variant