rs1064796453
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
|
27915094 |
2017 |
rs1064796453
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
|
28575650 |
2017 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
|
28575650 |
2017 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
|
27915094 |
2017 |
rs1553632361
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
|
28575650 |
2017 |
rs1553632361
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
|
27915094 |
2017 |
rs775104326
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
|
27915094 |
2017 |
rs775104326
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
|
28575650 |
2017 |
rs778624338
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
|
28575650 |
2017 |
rs778624338
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
|
27915094 |
2017 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
|
27915094 |
2017 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
|
28575650 |
2017 |
rs1064796453
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs1064796453
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
|
25326669 |
2015 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
|
25326669 |
2015 |
rs1553632361
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
|
25326669 |
2015 |
rs1553632361
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs775104326
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
|
25326669 |
2015 |
rs775104326
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs778624338
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs778624338
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
|
25326669 |
2015 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
|
25326669 |
2015 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs1064796453
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features.
|
24614104 |
2014 |