ClinVar Miner

List of variants in gene GDAP1 reported as benign for not provided

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Gene type:
ClinVar version:
Total variants: 36
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HGVS dbSNP gnomAD frequency
NM_018972.4(GDAP1):c.694+24C>T rs4463412 0.99998
NM_018972.4(GDAP1):c.*797A>G rs7007283 0.99369
NM_018972.2(GDAP1):c.-161G>T rs4541908 0.99275
NM_018972.4(GDAP1):c.484+182C>A rs4310196 0.48408
NM_018972.4(GDAP1):c.311-85T>C rs3780014 0.47917
NM_018972.4(GDAP1):c.117+339C>A rs12545409 0.34325
NM_018972.4(GDAP1):c.*1855A>G rs6472842 0.29968
NM_018972.4(GDAP1):c.118-233A>T rs3739345 0.29721
NM_018972.4(GDAP1):c.117+244C>T rs4415302 0.29439
NM_018972.4(GDAP1):c.507T>G (p.Ser169=) rs11554166 0.27295
NM_018972.4(GDAP1):c.*2214A>G rs10504580 0.26909
NM_018972.4(GDAP1):c.485-186A>G rs55894757 0.23044
NM_018972.4(GDAP1):c.579+119_579+120del rs3832592 0.22925
NM_018972.4(GDAP1):c.*1878G>T rs16938896 0.18836
NM_018972.4(GDAP1):c.*357A>G rs1135715 0.18199
NM_018972.4(GDAP1):c.*830C>G rs4737414 0.18198
NM_018972.4(GDAP1):c.310+243_310+244del rs10532467 0.14705
NM_018972.4(GDAP1):c.*1173G>T rs72665430 0.06104
NM_018972.4(GDAP1):c.695-309C>T rs4464961 0.05593
NM_018972.4(GDAP1):c.485-20C>G rs73345392 0.04498
NM_018972.4(GDAP1):c.694+75A>G rs16938895 0.04488
NM_018972.4(GDAP1):c.*1489del rs34856543 0.04395
NM_018972.4(GDAP1):c.311-126A>G rs11987378 0.02529
NM_018972.4(GDAP1):c.*1647C>T rs115466662 0.02466
NM_018972.4(GDAP1):c.118-87G>A rs116253195 0.02454
NC_000008.11:g.74350331A>T rs146798895 0.01914
NM_018972.4(GDAP1):c.311-185A>G rs11987371 0.01532
NM_018972.4(GDAP1):c.*561C>G rs80136809 0.00699
NM_018972.4(GDAP1):c.248G>C (p.Gly83Ala) rs371138642 0.00004
NC_000008.11:g.74350213_74350216dup rs112601241
NC_000008.11:g.74350214_74350216dup rs112601241
NC_000008.11:g.74350216dup rs112601241
NM_018972.4(GDAP1):c.-51_-49del rs201803887
NM_018972.4(GDAP1):c.311-146_311-143del rs10557622
NM_018972.4(GDAP1):c.485-238C>A rs138137016
NM_018972.4(GDAP1):c.580-167CT[8] rs140955331

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