ClinVar Miner

List of variants in gene LMOD3 reported as likely benign by GeneDx

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Gene type:
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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_198271.5(LMOD3):c.1226A>G (p.Gln409Arg) rs116257053 0.01432
NM_198271.5(LMOD3):c.1679C>T (p.Ala560Val) rs17005363 0.01235
NM_198271.5(LMOD3):c.1657-253C>T rs115631248 0.00952
NM_198271.5(LMOD3):c.1657-161T>C rs115107879 0.00949
NM_198271.5(LMOD3):c.1657-129A>G rs114228075 0.00912
NM_198271.5(LMOD3):c.1657-181T>C rs144725658 0.00526
NM_198271.5(LMOD3):c.1313A>T (p.Lys438Met) rs6810145 0.00516
NM_198271.5(LMOD3):c.1493G>A (p.Arg498Gln) rs116440123 0.00513
NM_198271.5(LMOD3):c.*255C>T rs188468021 0.00493
NM_198271.5(LMOD3):c.1257G>C (p.Met419Ile) rs75713718 0.00383
NM_198271.5(LMOD3):c.1656+145A>G rs139784452 0.00166
NM_198271.5(LMOD3):c.1190A>G (p.Gln397Arg) rs199592188 0.00163
NM_198271.5(LMOD3):c.837G>A (p.Lys279=) rs185967498 0.00138
NM_198271.5(LMOD3):c.1519G>A (p.Glu507Lys) rs149196259 0.00054
NM_198271.5(LMOD3):c.1353A>G (p.Pro451=) rs756048205 0.00003
NM_198271.5(LMOD3):c.426A>C (p.Glu142Asp) rs111848977
NM_198271.5(LMOD3):c.426A>G (p.Glu142=) rs111848977
NM_198271.5(LMOD3):c.456TGA[3] (p.Asp157del) rs752238157
NM_198271.5(LMOD3):c.788T>C (p.Ile263Thr) rs9835034

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