ClinVar Miner

List of variants in gene FGD4 reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP
NM_001304481.1(FGD4):c.220C>A (p.Pro74Thr) rs199744649
NM_001370298.3(FGD4):c.1961A>G (p.Gln654Arg)
NM_001370298.3(FGD4):c.2509C>A (p.Pro837Thr)
NM_139241.3(FGD4):c.1097T>C (p.Leu366Ser) rs555510533
NM_139241.3(FGD4):c.1366C>A (p.Pro456Thr) rs138160928
NM_139241.3(FGD4):c.1560C>A (p.Ile520=) rs61748364
NM_139241.3(FGD4):c.1878A>C (p.Glu626Asp)
NM_139241.3(FGD4):c.2149G>A (p.Val717Met) rs61753359
NM_139241.3(FGD4):c.329T>C (p.Leu110Pro) rs142609007
NM_139241.3(FGD4):c.597G>C (p.Met199Ile) rs1592295526
NM_139241.3(FGD4):c.998A>G (p.Gln333Arg) rs200149526

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.