rs879255516
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
MENTAL RETARDATION, AUTOSOMAL DOMINANT 21
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1215280530
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Mammary Neoplasms
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs1243010179
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Nephroblastoma
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs1567608876
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
MENTAL RETARDATION, AUTOSOMAL DOMINANT 21
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1567609067
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
MENTAL RETARDATION, AUTOSOMAL DOMINANT 21
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs879255570
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
MENTAL RETARDATION, AUTOSOMAL DOMINANT 21
|
CT |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs879255571
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
MENTAL RETARDATION, AUTOSOMAL DOMINANT 21
|
GA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1555534067
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
CTCF: insights into insulator function during development.
|
22354838 |
2012 |
rs1555534147
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
C |
0.700 |
CausalMutation |
CLINVAR |
CTCF: insights into insulator function during development.
|
22354838 |
2012 |
rs1555534189
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Muscle hypotonia
|
G |
0.700 |
GeneticVariation |
CLINVAR |
CTCF: insights into insulator function during development.
|
22354838 |
2012 |
rs1555534189
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
G |
0.700 |
GeneticVariation |
CLINVAR |
CTCF: insights into insulator function during development.
|
22354838 |
2012 |
rs1555535739
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Movement Disorders
|
T |
0.700 |
CausalMutation |
CLINVAR |
CTCF: insights into insulator function during development.
|
22354838 |
2012 |
rs1555535739
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Multiple congenital anomalies
|
T |
0.700 |
CausalMutation |
CLINVAR |
CTCF: insights into insulator function during development.
|
22354838 |
2012 |
rs1555535739
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
T |
0.700 |
CausalMutation |
CLINVAR |
CTCF: insights into insulator function during development.
|
22354838 |
2012 |
rs1555534067
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
CTCF: master weaver of the genome.
|
19563753 |
2009 |
rs1555534147
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
C |
0.700 |
CausalMutation |
CLINVAR |
CTCF: master weaver of the genome.
|
19563753 |
2009 |
rs1555534189
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Muscle hypotonia
|
G |
0.700 |
GeneticVariation |
CLINVAR |
CTCF: master weaver of the genome.
|
19563753 |
2009 |
rs1555534189
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
G |
0.700 |
GeneticVariation |
CLINVAR |
CTCF: master weaver of the genome.
|
19563753 |
2009 |
rs1555535739
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Movement Disorders
|
T |
0.700 |
CausalMutation |
CLINVAR |
CTCF: master weaver of the genome.
|
19563753 |
2009 |
rs1555535739
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Multiple congenital anomalies
|
T |
0.700 |
CausalMutation |
CLINVAR |
CTCF: master weaver of the genome.
|
19563753 |
2009 |
rs1555535739
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
T |
0.700 |
CausalMutation |
CLINVAR |
CTCF: master weaver of the genome.
|
19563753 |
2009 |
rs879255516
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
MENTAL RETARDATION, AUTOSOMAL DOMINANT 21
|
|
0.800 |
GeneticVariation |
UNIPROT |
De novo mutations in the genome organizer CTCF cause intellectual disability.
|
23746550 |
2013 |
rs1555534067
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
A |
0.700 |
CausalMutation |
CLINVAR |
De novo mutations in the genome organizer CTCF cause intellectual disability.
|
23746550 |
2013 |
rs1555534147
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Dysmorphic features
|
C |
0.700 |
CausalMutation |
CLINVAR |
De novo mutations in the genome organizer CTCF cause intellectual disability.
|
23746550 |
2013 |
rs1555534189
|
Entrez Id: |
10664 |
Gene Symbol: |
CTCF |
CTCF
|
Muscle hypotonia
|
G |
0.700 |
GeneticVariation |
CLINVAR |
De novo mutations in the genome organizer CTCF cause intellectual disability.
|
23746550 |
2013 |