ClinVar Miner

List of variants in gene FGD4 reported as benign for Charcot-Marie-Tooth disease type 4H

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 51
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001370298.3(FGD4):c.*4991A>G rs1239830 0.98950
NM_001370298.3(FGD4):c.*4438A>G rs11052124 0.51218
NM_001370298.3(FGD4):c.*5198G>A rs1133509 0.48630
NM_001370298.3(FGD4):c.*3770G>T rs11052123 0.45391
NM_001370298.3(FGD4):c.42C>G (p.Ile14Met) rs2651369 0.45332
NM_001370298.3(FGD4):c.1248-37T>A rs4931641 0.42297
NM_001370298.3(FGD4):c.*1492T>G rs7980205 0.34985
NM_001370298.3(FGD4):c.*1133A>C rs10844268 0.34952
NM_001370298.3(FGD4):c.2046+37A>G rs7970584 0.34250
NM_001370298.3(FGD4):c.*1454A>G rs7964947 0.31826
NM_001370298.3(FGD4):c.1716G>A (p.Arg572=) rs10844253 0.27488
NM_001370298.3(FGD4):c.1929G>A (p.Ala643=) rs11052110 0.25239
NM_001370298.3(FGD4):c.2047-7T>C rs11052113 0.15104
NM_001370298.3(FGD4):c.*1148C>T rs56110646 0.09020
NM_001370298.3(FGD4):c.*1723C>T rs4931030 0.08965
NM_001370298.3(FGD4):c.*1828A>T rs4931031 0.08944
NM_001370298.3(FGD4):c.1750-12C>T rs73083501 0.08851
NM_001370298.3(FGD4):c.1404+8G>A rs12823621 0.07737
NM_001370298.3(FGD4):c.167-61986C>T rs11052033 0.05001
NM_001370298.3(FGD4):c.*3630T>C rs73313005 0.03331
NM_001370298.3(FGD4):c.*4128C>T rs12312970 0.03301
NM_001370298.3(FGD4):c.*4652T>C rs16920125 0.02543
NM_001370298.3(FGD4):c.*4211T>C rs75583772 0.02209
NM_001370298.3(FGD4):c.1926T>C (p.Ser642=) rs60803891 0.01632
NM_001370298.3(FGD4):c.*2203T>C rs41276678 0.01601
NM_001370298.3(FGD4):c.1954-8T>C rs115061722 0.01466
NM_001370298.3(FGD4):c.*4454G>A rs147515673 0.01373
NM_001370298.3(FGD4):c.*3340A>C rs75320947 0.01342
NM_001370298.3(FGD4):c.167-61799G>C rs77113168 0.01285
NM_001370298.3(FGD4):c.*1007G>A rs114843464 0.01214
NM_001370298.3(FGD4):c.*22G>A rs114284024 0.01129
NM_001370298.3(FGD4):c.*4063A>G rs62642552 0.00933
NM_001370298.3(FGD4):c.*792A>T rs140601094 0.00932
NM_001370298.3(FGD4):c.1247+10G>T rs41276676 0.00792
NM_001370298.3(FGD4):c.1470C>T (p.Pro490=) rs16920084 0.00752
NM_001370298.3(FGD4):c.*4192G>T rs77065831 0.00605
NM_001370298.3(FGD4):c.*290G>A rs79732949 0.00603
NM_001370298.3(FGD4):c.1971C>T (p.Ile657=) rs61748364 0.00526
NM_001370298.3(FGD4):c.1143G>A (p.Ser381=) rs34555341 0.00517
NM_001370298.3(FGD4):c.*27G>A rs150192477 0.00475
NM_001370298.3(FGD4):c.*1564T>C rs77836862 0.00383
NM_001370298.3(FGD4):c.*4956T>A rs149215917 0.00361
NM_001370298.3(FGD4):c.2070C>G (p.Ala690=) rs188104446 0.00106
NM_001370298.3(FGD4):c.*1068A>G rs537833755 0.00075
NM_001370298.3(FGD4):c.*4988G>A rs540366205 0.00068
NM_001370298.3(FGD4):c.*1954A>G rs1239829
NM_001370298.3(FGD4):c.*2537C>A rs115173894
NM_001370298.3(FGD4):c.*3130G>A rs73087441
NM_001370298.3(FGD4):c.*3130G>T rs73087441
NM_001370298.3(FGD4):c.846C>G (p.Asp282Glu) rs904582
NM_001370298.3(FGD4):c.846C>T (p.Asp282=) rs904582

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.