{{Rsnum
|rsid=118203396
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TSC1
|position=132921943
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TSC1
}}{{omim
|id=605284
|rsnum=118203396
|variant=0009
}}{{ClinVar
|rsid=118203396
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=135797330
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=TSC1:7248
|GENE_NAME=TSC1
|GENE_ID=7248
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.135797330A>G
|CLNSRC=OMIM Allelic Variant; Tuberous sclerosis database (TSC1)
|CLNORIGIN=1
|CLNSRCID=605284.0009; TSC1_00411
|CLNSIG=5
|CLNCUI=C1854465
|CLNDBN=Tuberous sclerosis 1; Tuberous sclerosis syndrome
|Disease=Tuberous sclerosis 1; Tuberous sclerosis syndrome
|CLNACC=RCV000005412.1; RCV000042306.2
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1220:C1854465:191100:805; NBK1220:C0041341:191100:7199000
}}{{PMID|18830229|OA=1
}} Missense mutations to the TSC1 gene cause tuberous sclerosis complex.