List of variants reported as likely pathogenic for Fanconi anemia complementation group I by Fulgent Genetics, Fulgent Genetics

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

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001113378.2(FANCI):c.3622_3623del (p.Leu1208fs)	rs1491132258	0.00003
NM_001113378.2(FANCI):c.1804C>T (p.Arg602Ter)	rs1432325198	0.00002
NM_001113378.2(FANCI):c.3676dup (p.Thr1226fs)	rs773847168	0.00002
NM_001113378.2(FANCI):c.2568_2569del (p.Gly857fs)	rs1385885533	0.00001
NM_001113378.2(FANCI):c.2858dup (p.Arg954fs)	rs2054482551
NM_001113378.2(FANCI):c.3118_3119del (p.Lys1040fs)	rs907106559
NM_001113378.2(FANCI):c.3119del (p.Lys1040fs)	rs1596324325
NM_001113378.2(FANCI):c.3895C>T (p.Arg1299Ter)	rs551305056
NM_001113378.2(FANCI):c.998C>A (p.Ser333Ter)	rs761982725

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.