Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei. 1423634

1992

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Predictive motifs derived from cytosine methyltransferases. 2717398

1989

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 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: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Cloning, expression and chromosome locations of the human DNMT3 gene family. 10433969

1999

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. 10555141

1999

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. 10647011

1999

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 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: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 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: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR The human DNA methyltransferases DNMT3A and DNMT3B have two types of promoters with different CpG contents. 12359337

2002

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR The Tudor domain 'Royal Family': Tudor, plant Agenet, Chromo, PWWP and MBT domains. 12575993

2003

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Windows for sex-specific methylation marked by DNA methyltransferase expression profiles in mouse germ cells. 15063176

2004

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Dynamic expression of de novo DNA methyltransferases Dnmt3a and Dnmt3b in the central nervous system. 15672446

2005

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR DNA methyltransferase expression in the mouse germ line during periods of de novo methylation. 15739230

2005

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR The Polycomb group protein EZH2 directly controls DNA methylation. 16357870

2006

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Roles for Dnmt3b in mammalian development: a mouse model for the ICF syndrome. 16501171

2006

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Dynamic expression of DNMT3a and DNMT3b isoforms during male germ cell development in the mouse. 16725135

2006

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Coordinate regulation of DNA methyltransferase expression during oogenesis. 17445268

2007

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 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: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. 19344873

2009

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR The NCBI BioSystems database. 19854944

2010

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons. 20228804

2010

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Dnmt3a-dependent nonpromoter DNA methylation facilitates transcription of neurogenic genes. 20651149

2010

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR Dnmt3a regulates emotional behavior and spine plasticity in the nucleus accumbens. 20729844

2010

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR DNMT3A mutations in acute myeloid leukemia. 21067377

2010

dbSNP: rs147001633
rs147001633
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features
T 0.700 CausalMutation CLINVAR The DNMT3 family of mammalian de novo DNA methyltransferases. 21507354

2011