Submission Details

Submitter:

Classification:
Definitive
GENCC:100001
Gene:
Disease:
Fanconi anemia complementation group A
Fanconi anemia, complementation group A
Mode Of Inheritance:
Autosomal recessive
Evaluated Date:
01/28/2025
PubMed IDs:
12447395 12827451 10431244 8896564 15523645 11344308 10090479 10862090 11091222 12955722 15162062 15522956 15643609 15917947 16532972 21519011 23898106 24689079 24704046 26799702 27121516 29098742 29269525 29400309 29702541 30032139
Public Report:
Assertion Criteria:
Submitter Submitted Date:
07/02/2025

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.