ClinVar Miner

List of variants in gene FANCL reported as benign for DNA repair disease

Included ClinVar conditions (106):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
NM_001114636.1(FANCL):c.-39A>G rs41281511
NM_001114636.1(FANCL):c.108C>G (p.Phe36Leu) rs149726602
NM_001114636.1(FANCL):c.112C>T (p.Leu38Phe) rs55849827
NM_001114636.1(FANCL):c.217-11T>C rs79588315
NM_001114636.1(FANCL):c.402T>C (p.Ser134=) rs145284589
NM_001114636.1(FANCL):c.685A>G (p.Thr229Ala) rs149731356

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. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.