rs121909238
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.
|
26637798 |
2015 |
rs121909239
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.
|
26637798 |
2015 |
rs121909240
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.
|
26637798 |
2015 |
rs397514559
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.
|
26637798 |
2015 |
rs397514560
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Targeted DNA Sequencing from Autism Spectrum Disorder Brains Implicates Multiple Genetic Mechanisms.
|
26637798 |
2015 |
rs121909238
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
|
15805158 |
2005 |
rs121909239
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
|
15805158 |
2005 |
rs121909240
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
|
15805158 |
2005 |
rs397514559
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
|
15805158 |
2005 |
rs397514560
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations.
|
15805158 |
2005 |
rs121909231
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations.
|
24778394 |
2014 |
rs121913293
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Second malignant neoplasms in patients with Cowden syndrome with underlying germline PTEN mutations.
|
24778394 |
2014 |
rs121909227
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
|
25525159 |
2015 |
rs121913293
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
PTEN hamartoma tumor syndrome and Gorham-Stout phenomenon.
|
22628360 |
2012 |
rs121909227
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features.
|
21659347 |
2011 |
rs121909227
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.
|
9832032 |
1998 |
rs121913293
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutations in Epigenetic Regulation Genes Are a Major Cause of Overgrowth with Intellectual Disability.
|
28475857 |
2017 |
rs121909238
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
|
23160955 |
2012 |
rs121909239
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
|
23160955 |
2012 |
rs121909240
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
|
23160955 |
2012 |
rs397514559
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
|
23160955 |
2012 |
rs397514560
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
|
23160955 |
2012 |
rs121909227
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
|
23160955 |
2012 |
rs797045066
|
|
CA |
0.700 |
CausalMutation |
CLINVAR |
Molecular diagnostic experience of whole-exome sequencing in adult patients.
|
26633545 |
2016 |
rs1064793345
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Lifetime cancer risks in individuals with germline PTEN mutations.
|
22252256 |
2012 |