rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
CausalMutation |
CLINVAR |
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
|
24362816 |
2014 |
rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
LOVD v.2.0: the next generation in gene variant databases.
|
21520333 |
2011 |
rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2.
|
19669161 |
2010 |
rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
CausalMutation |
CLINVAR |
Comparative in silico analyses and experimental validation of novel splice site and missense mutations in the genes MLH1 and MSH2.
|
19669161 |
2010 |
rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of HNPCC-related missense mutations in MSH2.
|
18822302 |
2008 |
rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Functional analysis of HNPCC-related missense mutations in MSH2.
|
18822302 |
2008 |
rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.
|
15849733 |
2005 |
rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
CausalMutation |
CLINVAR |
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.
|
15849733 |
2005 |
rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
T |
0.700 |
CausalMutation |
CLINVAR |
Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer.
|
9774676 |
1998 |
rs267607950
|
Entrez Id: |
4436 |
Gene Symbol: |
MSH2 |
MSH2
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
A |
0.700 |
CausalMutation |
CLINVAR |
Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer.
|
9774676 |
1998 |