rs1555926209
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Prevalence and architecture of de novo mutations in developmental disorders.
|
28135719 |
2017 |
rs1555925903
|
|
Dysmorphic features
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Prevalence and architecture of de novo mutations in developmental disorders.
|
28135719 |
2017 |
rs1555923822
|
|
Dysmorphic features
|
CT |
0.700 |
CausalMutation
|
CLINVAR |
Prevalence and architecture of de novo mutations in developmental disorders.
|
28135719 |
2017 |
rs1555926209
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.
|
27479843 |
2016 |
rs1555925903
|
|
Dysmorphic features
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.
|
27479843 |
2016 |
rs1555923822
|
|
Dysmorphic features
|
CT |
0.700 |
CausalMutation
|
CLINVAR |
Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.
|
27479843 |
2016 |
rs1555926209
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs1555925903
|
|
Dysmorphic features
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs1555923822
|
|
Dysmorphic features
|
CT |
0.700 |
CausalMutation
|
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
rs1555926209
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Genome-wide atlas of gene expression in the adult mouse brain.
|
17151600 |
2007 |
rs1555925903
|
|
Dysmorphic features
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Genome-wide atlas of gene expression in the adult mouse brain.
|
17151600 |
2007 |
rs1555923822
|
|
Dysmorphic features
|
CT |
0.700 |
CausalMutation
|
CLINVAR |
Genome-wide atlas of gene expression in the adult mouse brain.
|
17151600 |
2007 |
rs1555926209
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
Discovery of transcription factors and other candidate regulators of neural crest development.
|
18351660 |
2008 |
rs1555925903
|
|
Dysmorphic features
|
T |
0.700 |
CausalMutation
|
CLINVAR |
Discovery of transcription factors and other candidate regulators of neural crest development.
|
18351660 |
2008 |
rs1555923822
|
|
Dysmorphic features
|
CT |
0.700 |
CausalMutation
|
CLINVAR |
Discovery of transcription factors and other candidate regulators of neural crest development.
|
18351660 |
2008 |
rs1555926209
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.
|
27436265 |
2016 |
rs1555925903
|
|
Dysmorphic features
|
T |
0.700 |
CausalMutation
|
CLINVAR |
De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.
|
27436265 |
2016 |
rs1555923822
|
|
Dysmorphic features
|
CT |
0.700 |
CausalMutation
|
CLINVAR |
De novo nonsense and frameshift variants of TCF20 in individuals with intellectual disability and postnatal overgrowth.
|
27436265 |
2016 |
rs1555926209
|
|
Dysmorphic features
|
A |
0.700 |
CausalMutation
|
CLINVAR |
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.
|
25228304 |
2014 |
rs1555925903
|
|
Dysmorphic features
|
T |
0.700 |
CausalMutation
|
CLINVAR |
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.
|
25228304 |
2014 |
rs1555923822
|
|
Dysmorphic features
|
CT |
0.700 |
CausalMutation
|
CLINVAR |
De novo and rare inherited mutations implicate the transcriptional coregulator TCF20/SPBP in autism spectrum disorder.
|
25228304 |
2014 |