Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Exome sequencing reveals DNMT3A and ASXL1 variants associate with progression of chronic myeloid leukemia after tyrosine kinase inhibitor therapy. 28667884

2017
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Tatton-Brown-Rahman syndrome due to 2p23 microdeletion. 26866722

2016
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Dnmt3a regulates emotional behavior and spine plasticity in the nucleus accumbens. 20729844

2010
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Windows for sex-specific methylation marked by DNA methyltransferase expression profiles in mouse germ cells. 15063176

2004
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons. 20228804

2010
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR The human DNA methyltransferases (DNMTs) 1, 3a and 3b: coordinate mRNA expression in normal tissues and overexpression in tumors. 10325416

1999
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Identification of De Novo DNMT3A Mutations That Cause West Syndrome by Using Whole-Exome Sequencing. 28386848

2018
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Detection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencing. 23849776

2013
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Cloning, expression and chromosome locations of the human DNMT3 gene family. 10433969

1999
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR DNA methylation in the human cerebral cortex is dynamically regulated throughout the life span and involves differentiated neurons. 17878930

2007
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. 10647011

1999
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei. 1423634

1992
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Enzymatic properties of recombinant Dnmt3a DNA methyltransferase from mouse: the enzyme modifies DNA in a non-processive manner and also methylates non-CpG [correction of non-CpA] sites. 11399089

2001
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. 19344873

2009
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR The NCBI BioSystems database. 19854944

2010
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR A novel Dnmt3a isoform produced from an alternative promoter localizes to euchromatin and its expression correlates with active de novo methylation. 12138111

2002
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR The DNMT3 family of mammalian de novo DNA methyltransferases. 21507354

2011
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability. 24614070

2014
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Dynamic expression of de novo DNA methyltransferases Dnmt3a and Dnmt3b in the central nervous system. 15672446

2005
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability. 28475857

2017
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. 10555141

1999
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR The Polycomb group protein EZH2 directly controls DNA methylation. 16357870

2006
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Coordinate regulation of DNA methyltransferase expression during oogenesis. 17445268

2007
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR De novo mutations revealed by whole-exome sequencing are strongly associated with autism. 22495306

2012
dbSNP: rs781139634
rs781139634
DNMT3A
A 0.700 CausalMutation CLINVAR Predictive motifs derived from cytosine methyltransferases. 2717398

1989