LGI1 Chromosome 10

Leucine rich glioma inactivated 1
85 variants 85 Health Risk

Upload your DNA to see your personal genotypes for variants in LGI1.

What This Gene Does
This gene encodes a member of the secreted leucine-rich repeat (LRR) superfamily and shares homology with members of the SLIT protein family. The encoded protein may regulate the activity of voltage-gated potassium channels and may be involved in neuronal growth regulation and cell survival. This gene is rearranged as a result of translocations in glioblastoma cell lines, and it is frequently down-regulated or rearranged in malignant gliomas. Mutations in this gene result in autosomal dominant lateral temporal epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
Gene Info
Gene Group
LGI family
Locus Type
gene with protein product
Location
10q23.33
Ensembl
ENSG00000108231
Associated Conditions (9)
Autosomal dominant epilepsy with auditory features
Inborn genetic diseases
Epilepsy
familial temporal lobe
1
LGI1-related disorder
Seizure
DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 121
Genitopatellar syndrome
Key Variants
RS1162193591
Conflicting classifications of pathogenicity
Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
Health Risk
RS1263918669
Conflicting classifications of pathogenicity
Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
Health Risk
RS140752487
Conflicting classifications of pathogenicity
Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
Health Risk
RS143808356
Conflicting classifications of pathogenicity
Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
Health Risk
RS145675377
Conflicting classifications of pathogenicity
Epilepsy, familial temporal lobe, 1
Health Risk
RS146425212
Conflicting classifications of pathogenicity
Epilepsy, familial temporal lobe, 1
Health Risk
RS147469708
Conflicting classifications of pathogenicity
Epilepsy, familial temporal lobe, 1
Health Risk
RS148263562
Conflicting classifications of pathogenicity
Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
Health Risk
RS148804268
Conflicting classifications of pathogenicity
Epilepsy, familial temporal lobe, 1
Health Risk
RS151104648
Conflicting classifications of pathogenicity
Epilepsy, familial temporal lobe, 1
Health Risk
RS201376381
Conflicting classifications of pathogenicity
Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
Health Risk
RS202148793
Conflicting classifications of pathogenicity
Epilepsy, familial temporal lobe, 1
Health Risk
All Variants (85)
RSID Category Clinical Significance Conditions
RS1162193591 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS1263918669 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS140752487 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS143808356 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS145675377 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS146425212 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS147469708 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS148263562 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS148804268 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS151104648 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS201376381 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS202148793 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS202204627 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS2059951179 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS370955995 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Autosomal dominant epilepsy with auditory features
RS373616721 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS376452111 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS544656851 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS587780379 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Autosomal dominant epilepsy with auditory features
RS748991956 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS755068491 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS761037722 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Autosomal dominant epilepsy with auditory features
RS768003944 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS770065197 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS772228851 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS777027658 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Autosomal dominant epilepsy with auditory features
RS777973395 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Autosomal dominant epilepsy with auditory features, Inborn genetic diseases
RS781205119 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Autosomal dominant epilepsy with auditory features
RS781404129 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS886047487 Health Risk Conflicting classifications of pathogenicity Epilepsy, familial temporal lobe, 1
RS934556455 Health Risk Conflicting classifications of pathogenicity Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS1064794249 Health Risk Likely pathogenic Autosomal dominant epilepsy with auditory features, Autosomal dominant epilepsy with auditory features
RS1064797149 Health Risk Likely pathogenic
RS1370527260 Health Risk Likely pathogenic Seizure, Seizure
RS1554905068 Health Risk Likely pathogenic
RS1564851314 Health Risk Likely pathogenic Autosomal dominant epilepsy with auditory features, Inborn genetic diseases, Autosomal dominant epilepsy with auditory features
RS2059583625 Health Risk Likely pathogenic Epilepsy, familial temporal lobe, 1
RS2059586444 Health Risk Likely pathogenic Epilepsy, familial temporal lobe, 1
RS2059593242 Health Risk Likely pathogenic Epilepsy, familial temporal lobe, 1
RS2134001459 Health Risk Likely pathogenic Epilepsy, familial temporal lobe, 1
RS2134020777 Health Risk Likely pathogenic Autosomal dominant epilepsy with auditory features, Autosomal dominant epilepsy with auditory features
RS2134020917 Health Risk Likely pathogenic Epilepsy, familial temporal lobe, 1
RS2134026453 Health Risk Likely pathogenic Epilepsy, familial temporal lobe, 1
RS2134027207 Health Risk Likely pathogenic
RS2492801872 Health Risk Likely pathogenic Epilepsy, familial temporal lobe, 1
RS2492904557 Health Risk Likely pathogenic Inborn genetic diseases, LGI1-related disorder, Inborn genetic diseases
RS2492905676 Health Risk Likely pathogenic Epilepsy, familial temporal lobe, 1
RS2492905831 Health Risk Likely pathogenic Epilepsy, familial temporal lobe, 1
RS2492917776 Health Risk Likely pathogenic
RS886039496 Health Risk Likely pathogenic Seizure, DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 121, Seizure
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