RS397509392 DNMT1

Health Risk Chr 19:10154709
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant cerebellar ataxia
deafness and narcolepsy
Hereditary sensory neuropathy-deafness-dementia syndrome
Inborn genetic diseases
Autosomal dominant cerebellar ataxia
deafness and narcolepsy
Hereditary sensory neuropathy-deafness-dementia syndrome
Inborn genetic diseases
Other Variants in DNMT1
rs199473690 rs199473691 rs397509391 rs397509393 rs199473692 rs146112081 rs141856197 rs148831705 rs138841970 rs201774098
Ask Dr. Hemsworth about this variant