rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
|
27915094 |
2017 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
|
28575650 |
2017 |
rs1553631783
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
|
28575650 |
2017 |
rs1553631783
|
|
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 |
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
|
28575650 |
2017 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Clinical features associated with CTNNB1 de novo loss of function mutations in ten individuals.
|
27915094 |
2017 |
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 |
rs1553631783
|
|
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 |
rs1553631783
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
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 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A new intellectual disability syndrome caused by CTNNB1 haploinsufficiency.
|
24668549 |
2014 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Chondrocyte β-catenin signaling regulates postnatal bone remodeling through modulation of osteoclast formation in a murine model.
|
24431282 |
2014 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features.
|
24614104 |
2014 |
rs1553631783
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Chondrocyte β-catenin signaling regulates postnatal bone remodeling through modulation of osteoclast formation in a murine model.
|
24431282 |
2014 |
rs1553631783
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features.
|
24614104 |
2014 |
rs1553631783
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
A new intellectual disability syndrome caused by CTNNB1 haploinsufficiency.
|
24668549 |
2014 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features.
|
24614104 |
2014 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
A new intellectual disability syndrome caused by CTNNB1 haploinsufficiency.
|
24668549 |
2014 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Chondrocyte β-catenin signaling regulates postnatal bone remodeling through modulation of osteoclast formation in a murine model.
|
24431282 |
2014 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in WNT1 cause different forms of bone fragility.
|
23499309 |
2013 |
rs1553631783
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations in WNT1 cause different forms of bone fragility.
|
23499309 |
2013 |
rs797044875
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Mutations in WNT1 cause different forms of bone fragility.
|
23499309 |
2013 |
rs1553631770
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Specific armadillo repeat sequences facilitate β-catenin nuclear transport in live cells via direct binding to nucleoporins Nup62, Nup153, and RanBP2/Nup358.
|
22110128 |
2012 |