ClinVar Miner

List of variants in gene FGD4 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
NM_001304481.1(FGD4):c.222C>A (p.Pro74=) rs1465471003
NM_139241.3(FGD4):c.-92-339A>G rs73305550
NM_139241.3(FGD4):c.1132+8_1132+9insG rs1555216986
NM_139241.3(FGD4):c.1398A>T (p.Thr466=) rs1220106574
NM_139241.3(FGD4):c.1431A>G (p.Lys477=) rs1023207495
NM_139241.3(FGD4):c.1494A>G (p.Thr498=) rs572887361
NM_139241.3(FGD4):c.1560C>T (p.Ile520=) rs61748364
NM_139241.3(FGD4):c.1635+221T>A rs12303795
NM_139241.3(FGD4):c.1711C>A (p.Pro571Thr) rs144693221
NM_139241.3(FGD4):c.1722A>G (p.Ala574=) rs771910342
NM_139241.3(FGD4):c.1758A>C (p.Gly586=) rs200761894
NM_139241.3(FGD4):c.1761+8A>T rs761674021
NM_139241.3(FGD4):c.1762-23T>G rs76834265
NM_139241.3(FGD4):c.2044-10T>C rs1592514932
NM_139241.3(FGD4):c.2214T>C (p.Ala738=) rs200144770
NM_139241.3(FGD4):c.236C>T (p.Thr79Ile) rs145115430
NM_139241.3(FGD4):c.255A>T (p.Ala85=) rs139357821
NM_139241.3(FGD4):c.57G>A (p.Lys19=) rs1427707678
NM_139241.3(FGD4):c.601-154T>G rs12299653
NM_139241.3(FGD4):c.759C>A (p.Ile253=) rs1592364946
NM_139241.3(FGD4):c.873A>G (p.Lys291=) rs1224103433

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.