rs1060500126
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1064793345
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Estimate of de novo mutation frequency in probands with PTEN hamartoma tumor syndrome.
|
22595938 |
2012 |
rs1064793345
|
|
C |
0.700 |
GeneticVariation |
CLINVAR |
Lifetime cancer risks in individuals with germline PTEN mutations.
|
22252256 |
2012 |
rs1085308041
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs1085308043
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs1114167621
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs1114167622
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs1114167640
|
|
CGCTT |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1114167650
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Characterization of cryptic splicing in germline PTEN intronic variants in Cowden syndrome.
|
28677221 |
2017 |
rs121909218
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909219
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909221
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909222
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909223
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909224
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations.
|
21956414 |
2011 |
rs121909224
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Autoimmunity, intestinal lymphoid hyperplasia, and defects in mucosal B-cell homeostasis in patients with PTEN hamartoma tumor syndrome.
|
22266152 |
2012 |
rs121909224
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.
|
9259288 |
1997 |
rs121909224
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Cognitive characteristics of PTEN hamartoma tumor syndromes.
|
23470840 |
2013 |
rs121909225
|
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909226
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909227
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909228
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909229
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs121909231
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN.
|
10353779 |
1999 |
rs121909231
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Incidence and clinical characteristics of thyroid cancer in prospective series of individuals with Cowden and Cowden-like syndrome characterized by germline PTEN, SDH, or KLLN alterations.
|
21956414 |
2011 |