MSH2 - Gene browser

MSH2

mutS homolog 2

HCNC Approved Symbol: MSH2 (HGNC:7325)
Genomic Coordinates: 2:47,403,067 - 47,709,830 (2p21-p16.3)
Synonyms: HNPCC, HNPCC1, MSH-2, COCA1
Disease Associations: This gene is associated with the following 3 diseases in OMIM.

12Patients

In total, 12 patients were diagnosed with a variant in the MSH2 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

012
Patient count

Colon cancer: 3 (25.0%)
Patient Count: 3 (25.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (25.0%)
Hereditary nonpolyposis colorectal carcinoma: 2 (16.7%)
Patient Count: 2 (16.7%)
% of total patients presenting each phenotype is shown in parentheses.
2 (16.7%)
Bladder cancer: 1 (8.3%)
Patient Count: 1 (8.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (8.3%)
Uterine cancer: 1 (8.3%)
Patient Count: 1 (8.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (8.3%)
Neoplasm of the rectum: 1 (8.3%)
Patient Count: 1 (8.3%)
% of total patients presenting each phenotype is shown in parentheses.
1 (8.3%)