DNMT3A, DNA methyltransferase 3 alpha, 1788

N. diseases: 350; N. variants: 56
Disease: Tatton Brown Rahman syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1164367418
rs1164367418
Entrez Id: 1788
Gene Symbol: DNMT3A
DNMT3A
CUI: C4014545
Disease:
Tatton Brown Rahman syndrome 		GC 0.700 CausalMutation CLINVAR