ClinVar Miner

List of variants in gene FGFR3 reported as likely benign by PreventionGenetics,PreventionGenetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
NM_000142.4(FGFR3):c.1534+15G>T rs367781042
NM_000142.4(FGFR3):c.1535-14C>T rs3135895
NM_000142.4(FGFR3):c.1959+8C>T rs371666188
NM_000142.4(FGFR3):c.2168+12C>T rs369096713
NM_000142.4(FGFR3):c.2274+50C>T rs756761813
NM_000142.4(FGFR3):c.616-14G>T rs886038256
NM_000142.4(FGFR3):c.616-6G>A rs17883400
NM_000142.4(FGFR3):c.740-9C>T rs886038257
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu) rs17881656
NM_000142.5(FGFR3):c.1223C>T (p.Ser408Phe) rs761877926
NM_000142.5(FGFR3):c.1227C>T (p.Pro409=) rs533316478
NM_000142.5(FGFR3):c.1290C>T (p.Ser430=) rs3135891
NM_000142.5(FGFR3):c.1332C>T (p.Ser444=) rs769521432
NM_000142.5(FGFR3):c.193G>A (p.Gly65Arg) rs2305178
NM_000142.5(FGFR3):c.894G>T (p.Val298=) rs886038258

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.