ClinVar Miner

List of variants reported as benign for Lissencephaly, Recessive

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Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_017668.3(NDE1):c.*202G>A rs11130 0.47916
NM_002474.3(MYH11):c.4242T>G (p.Ala1414=) rs2075511 0.45713
NM_002474.3(MYH11):c.3700G>A (p.Ala1234Thr) rs16967494 0.21955
NM_017668.3(NDE1):c.*947G>A rs760023 0.09015
NM_002474.3(MYH11):c.3967C>T (p.Leu1323=) rs12907 0.08987
NM_017668.3(NDE1):c.*913A>C rs760024 0.08447
NM_017668.3(NDE1):c.*1299A>G rs16967500 0.08018
NM_017668.3(NDE1):c.*1220G>A rs74009414 0.08006
NM_017668.3(NDE1):c.*1389G>A rs11557090 0.07983
NM_017668.3(NDE1):c.*1723C>T rs73519694 0.06691
NM_005045.4(RELN):c.-24GGC[10] (p.Met1_Glu2insGlyGly) rs55656324
NM_005045.4(RELN):c.4937-4dup rs35268159

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