Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
OMIM | RCV000018622 | SCV000038905 | pathogenic | Colorectal cancer, hereditary nonpolyposis, type 2 | 2001-06-01 | no assertion criteria provided | literature only | |
OMIM | RCV001267886 | SCV001446365 | pathogenic | Mismatch repair cancer syndrome 1 | 2001-06-01 | no assertion criteria provided | literature only |