DNMT1, DNA methyltransferase 1, 1786

N. diseases: 496; N. variants: 36
Disease: Hereditary Sensory and Autonomic Neuropathy Type Ie ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199473690
rs199473690
Entrez Id: 1786
Gene Symbol: DNMT1
DNMT1
CUI: C3279885
Disease:
Hereditary Sensory and Autonomic Neuropathy Type Ie 		0.800 GeneticVariation UNIPROT Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss. 21532572 2011
dbSNP: rs199473690
rs199473690
Entrez Id: 1786
Gene Symbol: DNMT1
DNMT1
CUI: C3279885
Disease:
Hereditary Sensory and Autonomic Neuropathy Type Ie 		C 0.800 GeneticVariation CLINVAR
dbSNP: rs199473690
rs199473690
Entrez Id: 1786
Gene Symbol: DNMT1
DNMT1
CUI: C3279885
Disease:
Hereditary Sensory and Autonomic Neuropathy Type Ie 		C 0.800 CausalMutation CLINVAR
dbSNP: rs199473691
rs199473691
Entrez Id: 1786
Gene Symbol: DNMT1
DNMT1
CUI: C3279885
Disease:
Hereditary Sensory and Autonomic Neuropathy Type Ie 		TAT 0.700 CausalMutation CLINVAR
dbSNP: rs199473692
rs199473692
Entrez Id: 1786
Gene Symbol: DNMT1
DNMT1
CUI: C3279885
Disease:
Hereditary Sensory and Autonomic Neuropathy Type Ie 		G 0.700 CausalMutation CLINVAR