ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 87
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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.1248-149T>G rs4931640 0.48473
NM_001370298.3(FGD4):c.2172+200G>A rs1909510 0.48266
NM_001370298.3(FGD4):c.1404+149T>C rs7964734 0.47160
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.1749+200A>C rs10844254 0.31222
NM_001370298.3(FGD4):c.1716G>A (p.Arg572=) rs10844253 0.27488
NM_001370298.3(FGD4):c.2455-236G>A rs10771973 0.26465
NM_001370298.3(FGD4):c.2173-257C>T rs11831099 0.26020
NM_001370298.3(FGD4):c.1544-135G>A rs10844252 0.25333
NM_001370298.3(FGD4):c.1929G>A (p.Ala643=) rs11052110 0.25239
NM_001370298.3(FGD4):c.167-83T>A rs61926167 0.22049
NM_001370298.3(FGD4):c.2313+77G>A rs59572242 0.20699
NM_001370298.3(FGD4):c.2047-7T>C rs11052113 0.15340
NM_001370298.3(FGD4):c.1750-142C>T rs112299849 0.15323
NM_001370298.3(FGD4):c.1922+215C>A rs12312688 0.15304
NM_001370298.3(FGD4):c.1922+202A>G rs12299270 0.15303
NM_001370298.3(FGD4):c.2047-292C>T rs11052111 0.15235
NM_001370298.3(FGD4):c.1954-144G>A rs12322190 0.15100
NM_001370298.3(FGD4):c.2455-227A>C rs56352987 0.10629
NM_001370298.3(FGD4):c.167-226G>A rs73305543 0.09839
NM_001370298.3(FGD4):c.1248-177G>A rs12298671 0.09803
NM_001370298.3(FGD4):c.2454+67G>A rs4575368 0.09035
NM_001370298.3(FGD4):c.*1148C>T rs56110646 0.09020
NM_001370298.3(FGD4):c.2313+246G>A rs113072835 0.09016
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.1954-21T>G rs17539792 0.08876
NM_001370298.3(FGD4):c.1544-42G>A rs1004969 0.08861
NM_001370298.3(FGD4):c.1404+8G>A rs12823621 0.07737
NM_001370298.3(FGD4):c.1011+89G>T rs12318679 0.05942
NM_001370298.3(FGD4):c.2455-46A>G rs74073032 0.05726
NM_001370298.3(FGD4):c.167-61986C>T rs11052033 0.04887
NM_001370298.3(FGD4):c.504-181G>A rs61926174 0.03557
NM_001370298.3(FGD4):c.1247+305C>G rs16920081 0.03166
NM_001370298.3(FGD4):c.1101+180A>G rs59670367 0.03081
NM_001370298.3(FGD4):c.2173-171G>C rs16920116 0.02993
NM_001370298.3(FGD4):c.2046+287C>T rs142904092 0.02944
NM_001370298.3(FGD4):c.2172+117G>T rs79100182 0.02587
NM_001370298.3(FGD4):c.504-145G>A rs75184912 0.02549
NM_001370298.3(FGD4):c.1012-262G>T rs74601811 0.02417
NM_001370298.3(FGD4):c.2047-125G>A rs139037931 0.02015
NM_001370298.3(FGD4):c.167-29719A>G rs17537634 0.01912
NM_001370298.3(FGD4):c.1926T>C (p.Ser642=) rs60803891 0.01632
NM_001370298.3(FGD4):c.2314-129C>T rs117293129 0.01602
NM_001370298.3(FGD4):c.1749+206A>T rs150202423 0.01462
NM_001370298.3(FGD4):c.2314-252A>G rs76880530 0.01435
NM_001370298.3(FGD4):c.1544-152T>A rs75906596 0.01421
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.*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.1971C>T (p.Ile657=) rs61748364 0.00526
NM_001370298.3(FGD4):c.*4956T>A rs149215917 0.00243
NM_001370298.3(FGD4):c.2560G>A (p.Val854Met) rs61753359 0.00131
NM_001370298.3(FGD4):c.*1954A>G rs1239829
NM_001370298.3(FGD4):c.*3130G>A rs73087441
NM_001370298.3(FGD4):c.*3130G>T rs73087441
NM_001370298.3(FGD4):c.1012-67G>A rs10437768
NM_001370298.3(FGD4):c.1544-236T>G rs1004968
NM_001370298.3(FGD4):c.167-111_167-106del rs371242429
NM_001370298.3(FGD4):c.1750-123T>C rs12319480
NM_001370298.3(FGD4):c.1953+40_1953+41dup rs10700807
NM_001370298.3(FGD4):c.1953+41dup rs10700807
NM_001370298.3(FGD4):c.2046+221_2046+222insTA rs368679104
NM_001370298.3(FGD4):c.2046+221del rs374139685
NM_001370298.3(FGD4):c.2046+221dup rs374139685
NM_001370298.3(FGD4):c.2047-138T>C rs11052112
NM_001370298.3(FGD4):c.2122C>A (p.Pro708Thr) rs144693221
NM_001370298.3(FGD4):c.2172+29T>G rs17539848
NM_001370298.3(FGD4):c.2173-322del rs150852537
NM_001370298.3(FGD4):c.2313+123T>C rs144028061
NM_001370298.3(FGD4):c.504-285AAAT[2] rs139928530
NM_001370298.3(FGD4):c.846C>G (p.Asp282Glu) rs904582
NM_001370298.3(FGD4):c.846C>T (p.Asp282=) rs904582

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