List of variants in gene combination FANCA, LOC132090450 reported as likely pathogenic for Fanconi anemia complementation group A

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.3382C>T (p.Gln1128Ter)	rs1439817346
NM_000135.4(FANCA):c.3393_3395delinsA (p.Ala1132fs)	rs2544120712
NM_000135.4(FANCA):c.3398del (p.His1133fs)	rs2038407878
NM_000135.4(FANCA):c.3400TTC[1] (p.Phe1135del)	rs786204246
NM_000135.4(FANCA):c.3402dup (p.Phe1135fs)	rs1555537347
NM_000135.4(FANCA):c.3409-25_3418del	rs2544119774

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.