RS397509393 DNMT1

Health Risk Chr 19:10154604
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant cerebellar ataxia
deafness and narcolepsy
Hereditary sensory neuropathy-deafness-dementia syndrome
Autosomal dominant cerebellar ataxia
deafness and narcolepsy
Hereditary sensory neuropathy-deafness-dementia syndrome
Other Variants in DNMT1
rs199473690 rs199473691 rs397509391 rs397509392 rs199473692 rs146112081 rs141856197 rs148831705 rs138841970 rs201774098
Ask Dr. Hemsworth about this variant