List of variants reported as benign for leukoencephalopathy, megalencephalic by Genome-Nilou Lab

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Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_015166.4(MLC1):c.321+50T>C	rs79301	0.94928
NM_015166.4(MLC1):c.526-118C>T	rs4838882	0.92209
NM_152722.5(HEPACAM):c.652A>G (p.Met218Val)	rs10790715	0.75929
NM_015166.4(MLC1):c.714+28G>A	rs2038048	0.37853
NM_015166.4(MLC1):c.895-139G>A	rs11568183	0.27262
NM_015166.4(MLC1):c.525+153G>A	rs6010166	0.23729
NM_015166.4(MLC1):c.*48A>G	rs137919	0.23521
NM_152722.5(HEPACAM):c.618C>T (p.Arg206=)	rs10790716	0.20834
NM_015166.4(MLC1):c.1059+16G>A	rs5771338	0.17531
NM_015166.4(MLC1):c.894+194G>A	rs2076127	0.16956
NM_015166.4(MLC1):c.*45A>G	rs2072873	0.14823
NM_015166.4(MLC1):c.525+22G>A	rs2072874	0.14143
NM_015166.4(MLC1):c.525+64G>A	rs2076137	0.14127
NM_015166.4(MLC1):c.771+175T>C	rs2076132	0.11786
NM_015166.4(MLC1):c.771+160T>C	rs2076133	0.11739
NM_015166.4(MLC1):c.771+59C>A	rs2076135	0.11739
NM_015166.4(MLC1):c.771+61T>C	rs2076134	0.11739
NM_015166.4(MLC1):c.772-35C>T	rs11568179	0.11738
NM_015166.4(MLC1):c.894+52T>C	rs5771349	0.11723
NM_015166.4(MLC1):c.894+199C>T	rs5771142	0.11704
NM_015166.4(MLC1):c.895-9C>T	rs11568185	0.11704
NM_015166.4(MLC1):c.895-23C>T	rs11568184	0.11703
NM_015166.4(MLC1):c.772-110A>G	rs111258391	0.11687
NM_015166.4(MLC1):c.597A>G (p.Ser199=)	rs6010164	0.11147
NM_015166.4(MLC1):c.594C>T (p.Tyr198=)	rs6010165	0.11145
NM_015166.4(MLC1):c.978C>T (p.Cys326=)	rs11568186	0.10918
NM_015166.4(MLC1):c.996T>C (p.Ser332=)	rs11568187	0.10904
NM_015166.4(MLC1):c.512G>T (p.Cys171Phe)	rs6010260	0.10037
NM_015166.4(MLC1):c.1031A>G (p.Asn344Ser)	rs11568188	0.09405
NM_015166.4(MLC1):c.771+158G>A	rs35480507	0.08730
NM_015166.4(MLC1):c.1059+27A>G	rs114282486	0.05667
NM_015166.4(MLC1):c.*55C>T	rs41283496	0.02067
NM_015166.4(MLC1):c.772-80C>G	rs75474964

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