ClinVar Miner

List of variants reported as benign for leukoencephalopathy, megalencephalic by Illumina Laboratory Services, Illumina

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_152722.5(HEPACAM):c.*1279A>G rs3802904 0.76330
NM_152722.5(HEPACAM):c.652A>G (p.Met218Val) rs10790715 0.75929
NM_015166.4(MLC1):c.*1127C>T rs9628320 0.24216
NM_015166.4(MLC1):c.*48A>G rs137919 0.23521
NM_152722.5(HEPACAM):c.618C>T (p.Arg206=) rs10790716 0.20834
NM_152722.5(HEPACAM):c.877+14C>T rs11826299 0.15246
NM_015166.4(MLC1):c.*45A>G rs2072873 0.14823
NM_015166.3(MLC1):c.-561G>A rs4838883 0.13827
NM_015166.4(MLC1):c.*1764G>T rs41283489 0.13206
NM_015166.4(MLC1):c.895-9C>T rs11568185 0.11704
NM_015166.4(MLC1):c.*991T>G rs11704648 0.11696
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.*937C>T rs41283491 0.10778
NM_015166.4(MLC1):c.512G>T (p.Cys171Phe) rs6010260 0.10037
NM_015166.4(MLC1):c.*1836G>A rs11703598 0.09905
NM_015166.4(MLC1):c.1031A>G (p.Asn344Ser) rs11568188 0.09405
NM_152722.5(HEPACAM):c.*1206T>A rs78859654 0.07422
NM_152722.5(HEPACAM):c.*338C>A rs75988347 0.06504
NM_152722.5(HEPACAM):c.971A>G (p.Asn324Ser) rs116102273 0.05505
NM_015166.4(MLC1):c.*1963C>G rs41283487 0.04214
NM_152722.5(HEPACAM):c.339G>A (p.Gln113=) rs74570840 0.02928
NM_152722.5(HEPACAM):c.363G>A (p.Glu121=) rs112686308 0.02736
NM_015166.4(MLC1):c.*55C>T rs41283496 0.02067
NM_015166.4(MLC1):c.*1143C>T rs2294384 0.01944
NM_152722.5(HEPACAM):c.*50C>G rs192160991 0.01463
NM_015166.4(MLC1):c.*970G>C rs117474715 0.01437
NM_015166.4(MLC1):c.*1773G>C rs80312581 0.01130
NM_015166.4(MLC1):c.*1334G>A rs2294382 0.01127
NM_015166.3(MLC1):c.-156C>T rs2076126 0.01015
NM_152722.5(HEPACAM):c.975G>A (p.Pro325=) rs116536622 0.00836
NM_015166.4(MLC1):c.*339C>T rs115770001 0.00833
NM_015166.4(MLC1):c.*572C>T rs367816647 0.00818
NM_015166.4(MLC1):c.*1321A>G rs149073568 0.00778
NM_015166.4(MLC1):c.*12G>A rs142027672 0.00776
NM_152722.5(HEPACAM):c.258G>A (p.Glu86=) rs35466065 0.00669
NM_015166.4(MLC1):c.932T>A (p.Val311Glu) rs141225099 0.00622
NM_015166.4(MLC1):c.216G>A (p.Leu72=) rs78365284 0.00499
NM_015166.4(MLC1):c.279G>A (p.Ser93=) rs11568172 0.00422
NM_152722.5(HEPACAM):c.*1614A>T rs79225627 0.00396
NM_152722.5(HEPACAM):c.288A>C (p.Arg96=) rs36089266 0.00382
NM_152722.5(HEPACAM):c.851A>G (p.Gln284Arg) rs77759828 0.00225
NM_015166.4(MLC1):c.1053T>C (p.Ala351=) rs11568190 0.00056
NM_015166.4(MLC1):c.*773G>A rs4838880 0.00039
NM_152722.5(HEPACAM):c.-28G>A rs146644154 0.00030
NM_015166.3(MLC1):c.-528dup rs137931
NM_015166.4(MLC1):c.*1623G>T rs35730155
NM_015166.4(MLC1):c.*661G>C rs376823805
NM_015166.4(MLC1):c.-59-14T>A rs141840641
NM_015166.4(MLC1):c.654C>A (p.Asn218Lys) rs41302601
NM_152722.5(HEPACAM):c.*112G>T rs10893303
NM_152722.5(HEPACAM):c.*1794GTTT[3] rs560243987

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