rs121909238
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121909239
|
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs121909240
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs397514559
|
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs397514560
|
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1057524874
|
|
GGA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1114167667
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909219
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909224
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1224040268
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1564568303
|
|
AAG |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs370795352
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs398123323
|
|
TA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs797045904
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs863224909
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs863224909
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909231
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis.
|
9399897 |
1997 |
rs121909227
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.
|
9832032 |
1998 |
rs121909231
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis.
|
10749983 |
2000 |
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 |
rs121913293
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Cowden syndrome and Bannayan Riley Ruvalcaba syndrome represent one condition with variable expression and age-related penetrance: results of a clinical study of PTEN mutation carriers.
|
17526800 |
2007 |