Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
Lynch syndrome 8
Lynch syndrome 8
Mode Of Inheritance:
Autosomal dominant
Evaluated Date:
11/08/2022
PubMed IDs:
18398828 19098912 19188665 19215248 19900449 20046825 20301390 21309036 21642682 23091106 23938213 26101330 26657901 27013479 28754778 28772289 31337882
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

The GenCC data are available free of restriction under a CC0 1.0 Universal (CC0 1.0) Public Domain Dedication. The GenCC requests that you give attribution to GenCC and the contributing sources whenever possible and appropriate. The accepted Flagship manuscript is now available from Genetics in Medicine (https://www.gimjournal.org/article/S1098-3600(22)00746-8/fulltext).

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. The GenCC does not independently verify the submitted information. Though the information is obtained from sources believed to be reliable, no warranty, expressed or implied, is made regarding accuracy, adequacy, completeness, reliability or usefulness of any information. This disclaimer applies to both isolated and aggregate uses of the information. The information is provided on an "as is" basis, collected through periodic submission and therefore may not represent the most up-to-date information from the submitters. If you have questions about the medical relevance of information contained on this website, please see a healthcare professional; if you have questions about specific gene-disease claims, please contact the relevant sources; and if you have questions about the representation of the data on this website, please contact gencc@thegencc.org.