ClinVar Miner

List of variants in gene GFM2 reported as likely pathogenic by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_032380.5(GFM2):c.569G>A (p.Arg190Gln) rs761283105 0.00003
NM_032380.5(GFM2):c.1220+2dup rs773010798 0.00002
NM_032380.5(GFM2):c.64-16_64-3del rs751852874 0.00001
NM_032380.5(GFM2):c.1688_1694del (p.Ala563fs)
NM_032380.5(GFM2):c.883del (p.Val295fs)

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.