← New search
Variant profile

L99A

L99A · SaudiVarKB evidence summary derived from retained literature mentions.

1Variant mentions
1Publications
1Associated gene records
2Associated phenotype records

Associated gene records

Co-mentioned in the same publications
GeneIdentifier / contextArticlesMentions
CFL1HGNC:187411

Associated phenotype records

Co-mentioned in the same publications
PhenotypeIdentifier / contextArticlesMentions
Alzheimer disease11
epilepsyHP:000125011

Associated population records

Co-mentioned in the same publications

No retained population associations.

Supporting publications

1 records
  1. 2022Identification of the most damaging nsSNPs in the human CFL1 gene and their functional and structural impacts on cofilin-1 protein.Gene1 mentions