ClinVar Miner

List of variants in gene PLOD3 reported as benign for not provided

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Gene type:
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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_001084.5(PLOD3):c.109+46G>A rs28361887 0.30154
NM_001084.5(PLOD3):c.-81A>G rs1056678 0.23397
NC_000007.14:g.101217932T>C rs17319250 0.23048
NM_001084.5(PLOD3):c.1935+200T>C rs7802724 0.19435
NM_001084.5(PLOD3):c.2061+12T>C rs4729671 0.19416
NM_001084.5(PLOD3):c.1789-239C>T rs77665329 0.09531
NM_001084.5(PLOD3):c.679+77G>A rs77576173 0.08340
NM_001084.5(PLOD3):c.1128-132C>G rs3213663 0.07091
NM_001084.5(PLOD3):c.1233-4G>A rs2301903 0.05322
NM_001084.5(PLOD3):c.1232+20C>T rs79137018 0.03295
NM_001084.5(PLOD3):c.570C>T (p.Asp190=) rs35159414 0.02885
NM_001084.5(PLOD3):c.1977C>T (p.Asp659=) rs11546151 0.01458
NM_001084.5(PLOD3):c.939C>T (p.Arg313=) rs1546840 0.01334
NM_001084.5(PLOD3):c.1788+50A>G rs77698195 0.01284
NM_001084.5(PLOD3):c.1512C>T (p.Leu504=) rs79729122 0.01283
NM_001084.5(PLOD3):c.1788+49C>T rs79700584 0.01282
NM_001084.5(PLOD3):c.1886C>T (p.Thr629Met) rs74498833 0.01200
NM_001084.5(PLOD3):c.1500+6C>T rs77805300 0.01141
NM_001084.5(PLOD3):c.1179C>T (p.Ala393=) rs11546152 0.00779
NM_001084.5(PLOD3):c.1144G>C (p.Asp382His) rs41281013 0.00583
NM_001084.5(PLOD3):c.1528C>T (p.His510Tyr) rs35929039 0.00447
NM_001084.5(PLOD3):c.1797G>A (p.Arg599=) rs139049819 0.00393
NM_001084.5(PLOD3):c.123G>A (p.Val41=) rs112321807 0.00313
NM_001084.5(PLOD3):c.535A>G (p.Ile179Val) rs34646598 0.00305
NM_001084.5(PLOD3):c.880-16G>A rs190246843 0.00241
NM_001084.5(PLOD3):c.1500+17G>A rs186225619 0.00227
NM_001084.5(PLOD3):c.1986G>A (p.Pro662=) rs117761436 0.00136
NM_001084.5(PLOD3):c.975C>T (p.Pro325=) rs141101386 0.00122
NM_001084.5(PLOD3):c.616-17C>T rs200794469 0.00103
NM_001084.5(PLOD3):c.1678G>C (p.Glu560Gln) rs140879834 0.00078
NM_001084.5(PLOD3):c.2061+7C>A rs544790895 0.00059
NM_001084.5(PLOD3):c.1684-13G>A rs185427705 0.00056
NM_001084.5(PLOD3):c.735C>T (p.Tyr245=) rs149684440 0.00054
NM_001084.5(PLOD3):c.1776C>T (p.Gly592=) rs145632943 0.00051
NM_001084.5(PLOD3):c.1466C>T (p.Pro489Leu) rs145508748 0.00044
NM_001084.5(PLOD3):c.988C>G (p.Leu330Val) rs143574903 0.00036
NM_001084.5(PLOD3):c.804C>T (p.Tyr268=) rs202155755 0.00034
NM_001084.5(PLOD3):c.2124A>G (p.Ala708=) rs201504279 0.00010
NM_001084.5(PLOD3):c.201+10G>A rs770754925 0.00003
NM_001084.5(PLOD3):c.812A>G (p.Asn271Ser) rs535949022 0.00003
NM_001084.5(PLOD3):c.201+20C>T rs534558868 0.00002
NM_001084.5(PLOD3):c.503-11C>T rs769006032 0.00001
NM_001084.5(PLOD3):c.679+19G>A rs540323862 0.00001
NM_001084.5(PLOD3):c.1232+13del
NM_001084.5(PLOD3):c.1233-34C>G rs2301904
NM_001084.5(PLOD3):c.1402C>G (p.Arg468Gly) rs75592752
NM_001084.5(PLOD3):c.1452C>G (p.Gly484=)
NM_001084.5(PLOD3):c.1501-8dup rs2116800287
NM_001084.5(PLOD3):c.1564G>A (p.Asp522Asn)
NM_001084.5(PLOD3):c.1615-13dup rs763197529
NM_001084.5(PLOD3):c.1683+143G>A rs7777930
NM_001084.5(PLOD3):c.1683+201A>G rs1468358
NM_001084.5(PLOD3):c.1935+13C>T
NM_001084.5(PLOD3):c.1935+51G>A rs117827620
NM_001084.5(PLOD3):c.2061+14AC[3] rs561008952
NM_001084.5(PLOD3):c.2061+50G>T rs80179986
NM_001084.5(PLOD3):c.2062-87C>T rs4729670
NM_001084.5(PLOD3):c.2109G>A (p.Pro703=)
NM_001084.5(PLOD3):c.993C>T (p.Phe331=) rs1546841

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