ClinVar Miner

List of variants in gene FGFR1 reported as likely benign for Kallmann syndrome 2; Pfeiffer syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
Download table as spreadsheet
NM_023110.2(FGFR1):c.1285-8C>A rs1235765985
NM_023110.2(FGFR1):c.2106C>T (p.Pro702=) rs777061347
NM_023110.2(FGFR1):c.2186+8C>T rs372639138
NM_023110.2(FGFR1):c.2464C>T (p.Arg822Cys) rs17182463
NM_023110.2(FGFR1):c.471C>G (p.Ser157=) rs376497452

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.