ClinVar Miner

List of variants reported as not provided for FOXG1 disorder

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
GRCh37/hg19 14q12(chr14:28688830-30017377)x1
NM_005249.5(FOXG1):c.1062del (p.Ser355fs) rs1881817310
NM_005249.5(FOXG1):c.136dup (p.Gln46fs) rs587783629
NM_005249.5(FOXG1):c.460dup (p.Glu154fs) rs398124204

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.