ClinVar Miner

List of variants in gene FIG4 reported as uncertain significance by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
NM_014845.5(FIG4):c.1051G>C (p.Asp351His) rs879253941
NM_014845.5(FIG4):c.1091T>A (p.Met364Lys) rs772677048
NM_014845.5(FIG4):c.1388+5G>T rs200730266
NM_014845.5(FIG4):c.1703A>G (p.Lys568Arg) rs1064797016
NM_014845.5(FIG4):c.2035C>T (p.Arg679Trp) rs188910818
NM_014845.5(FIG4):c.2080A>G (p.Met694Val) rs143531641
NM_014845.5(FIG4):c.2096G>A (p.Arg699His) rs750091928
NM_014845.5(FIG4):c.2200G>A (p.Glu734Lys) rs372846619
NM_014845.5(FIG4):c.2405A>G (p.Tyr802Cys) rs370293982
NM_014845.5(FIG4):c.2567C>T (p.Ser856Leu) rs200970494
NM_014845.5(FIG4):c.2639T>A (p.Ile880Asn) rs746915624
NM_014845.5(FIG4):c.263G>A (p.Arg88Gln) rs879254310
NM_014845.5(FIG4):c.506A>C (p.Tyr169Ser) rs770278572
NM_014845.5(FIG4):c.719G>C (p.Ser240Thr) rs772586786
NM_014845.5(FIG4):c.730C>T (p.Arg244Cys) rs138376077
NM_014845.6(FIG4):c.2433AGA[2] (p.Glu813del) rs876661144

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.