rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Patients with colorectal cancer associated with Lynch syndrome and MLH1 promoter hypermethylation have similar prognoses.
|
26866578 |
2016 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Screening for germline mismatch repair mutations following diagnosis of sebaceous neoplasm.
|
25006859 |
2014 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Inactivation of DNA mismatch repair by variants of uncertain significance in the PMS2 gene.
|
24027009 |
2013 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Inactivation of DNA mismatch repair by variants of uncertain significance in the PMS2 gene.
|
24027009 |
2013 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants.
|
23709753 |
2013 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants.
|
23709753 |
2013 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Recurrent and founder mutations in the PMS2 gene.
|
22577899 |
2013 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Recurrent and founder mutations in the PMS2 gene.
|
22577899 |
2013 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelines.
|
21376568 |
2011 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Pitfalls in molecular analysis for mismatch repair deficiency in a family with biallelic pms2 germline mutations.
|
21204794 |
2011 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Café-au-lait macules and pediatric malignancy caused by biallelic mutations in the DNA mismatch repair (MMR) gene PMS2.
|
18273873 |
2008 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Long-range PCR facilitates the identification of PMS2-specific mutations.
|
16619239 |
2006 |
rs121434629
|
Entrez Id: |
5395 |
Gene Symbol: |
PMS2 |
PMS2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Two PMS2 mutations in a Turcot syndrome family with small bowel cancers.
|
16144131 |
2005 |