ClinVar Miner

List of variants in gene combination FANCA, ZNF276 reported as 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: 9
Download table as spreadsheet
HGVS dbSNP
NM_000135.2(FANCA):c.*154G>A rs1230
NM_000135.2(FANCA):c.*673A>G rs62704561
NM_000135.2(FANCA):c.*673delA rs17233826
NM_000135.2(FANCA):c.3891G>A (p.Lys1297=) rs17227361
NM_000135.2(FANCA):c.3935-9G>A rs9282680
NM_000135.2(FANCA):c.4036G>A (p.Ala1346Thr) rs17227396
NM_000135.2(FANCA):c.4249C>G (p.His1417Asp) rs17227403
NM_000135.3(FANCA):c.4332T>G (p.Pro1444=) rs149531696
NM_001286167.2(FANCA):c.3859G>A (p.Val1287Ile) rs17227354

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.