List of variants in gene FAN1 reported as uncertain significance by GeneDx

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014967.5(FAN1):c.1111G>A (p.Gly371Ser)	rs142597944	0.00033
NM_014967.5(FAN1):c.1090A>C (p.Asn364His)	rs187082481	0.00013
NM_014967.5(FAN1):c.1270C>T (p.Arg424Cys)	rs368417113	0.00004
NM_014967.5(FAN1):c.-152-7_-152-5del	rs747665384
NM_014967.5(FAN1):c.1738G>A (p.Gly580Ser)
NM_014967.5(FAN1):c.560_561del (p.Thr187fs)	rs772700881
NM_014967.5(FAN1):c.706_709del (p.Ile236fs)

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.