ClinVar Miner

List of variants in gene FGD4 reported as benign for peripheral neuropathy

Included ClinVar conditions (517):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_001370298.3(FGD4):c.*4991A>G rs1239830 0.98871
NM_001370298.3(FGD4):c.*4438A>G rs11052124 0.51721
NM_001370298.3(FGD4):c.*5198G>A rs1133509 0.48969
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 0.34951
NM_001370298.3(FGD4):c.2046+37A>G rs7970584 0.34437
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 0.15340
NM_001370298.3(FGD4):c.*1148C>T rs56110646 0.09020
NM_001370298.3(FGD4):c.*1723C>T rs4931030 0.09014
NM_001370298.3(FGD4):c.*1828A>T rs4931031 0.08985
NM_001370298.3(FGD4):c.1750-12C>T rs73083501 0.08885
NM_001370298.3(FGD4):c.1404+8G>A rs12823621 0.07737
NM_001370298.3(FGD4):c.167-61986C>T rs11052033 0.04887
NM_001370298.3(FGD4):c.*3630T>C rs73313005 0.03542
NM_001370298.3(FGD4):c.*4128C>T rs12312970 0.03539
NM_001370298.3(FGD4):c.*4652T>C rs16920125 0.02707
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 0.01207
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.*290G>A rs79732949 0.00658
NM_001370298.3(FGD4):c.*4192G>T rs77065831 0.00605
NM_001370298.3(FGD4):c.1143G>A (p.Ser381=) rs34555341 0.00555
NM_001370298.3(FGD4):c.1971C>T (p.Ile657=) rs61748364 0.00526
NM_001370298.3(FGD4):c.*27G>A rs150192477 0.00475
NM_001370298.3(FGD4):c.*1564T>C rs77836862 0.00399
NM_001370298.3(FGD4):c.*4956T>A rs149215917 0.00243
NM_001370298.3(FGD4):c.1296C>T (p.Phe432=) rs151083690 0.00230
NM_001370298.3(FGD4):c.2070C>G (p.Ala690=) rs188104446 0.00106
NM_001370298.3(FGD4):c.1075G>A (p.Val359Ile) rs528790143 0.00050
NM_001370298.3(FGD4):c.785C>T (p.Thr262Met) rs200732890 0.00030
NM_001370298.3(FGD4):c.*4988G>A rs540366205 0.00003
NM_001370298.3(FGD4):c.*1068A>G rs537833755 0.00002
NM_001370298.3(FGD4):c.*1954A>G rs1239829
NM_001370298.3(FGD4):c.*2537C>A rs115173894
NM_001370298.3(FGD4):c.*2928_*2931del rs549931906
NM_001370298.3(FGD4):c.*3130G>A rs73087441
NM_001370298.3(FGD4):c.*3130G>T rs73087441
NM_001370298.3(FGD4):c.*3148del rs797002948
NM_001370298.3(FGD4):c.*4369dup rs35874340
NM_001370298.3(FGD4):c.1543+17dup rs548627916
NM_001370298.3(FGD4):c.2122C>A (p.Pro708Thr) rs144693221
NM_001370298.3(FGD4):c.846C>G (p.Asp282Glu) rs904582
NM_001370298.3(FGD4):c.846C>T (p.Asp282=) rs904582

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