ClinVar Miner

List of variants in gene FANCL reported as likely benign for Fanconi anemia complementation group A

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_018062.3(FANCL):c.155+7T>C rs200849840
NM_018062.3(FANCL):c.156-8A>C rs878855045
NM_018062.3(FANCL):c.203G>C (p.Arg68Pro) rs143819820
NM_018062.3(FANCL):c.217-11T>C rs79588315
NM_018062.3(FANCL):c.273+7A>C rs745366278
NM_018062.3(FANCL):c.387G>A (p.Ala129=) rs141400460
NM_018062.3(FANCL):c.51C>G (p.Pro17=) rs772700022
NM_018062.3(FANCL):c.534A>G (p.Thr178=) rs151181785
NM_018062.3(FANCL):c.670A>G (p.Thr224Ala) rs149731356
NM_018062.3(FANCL):c.81A>C (p.Gly27=) rs1553459821
NM_018062.3(FANCL):c.96+10C>T rs184741617

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.