{{Rsnum
|rsid=45483392
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TSC2
|position=2087897
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TSC2
}}{{omim
|id=191092
|rsnum=45483392
|variant=0009
}}

{{ClinVar
|rsid=45483392
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=2137898
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=TSC2:7249
|GENE_NAME=TSC2
|GENE_ID=7249
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.2137898C>T
|CLNSRC=OMIM Allelic Variant; Tuberous sclerosis database (TSC2)
|CLNORIGIN=1
|CLNSRCID=191092.0009; TSC2_00033
|CLNSIG=5
|CLNCUI=C1860707
|CLNDBN=Tuberous sclerosis 2; Tuberous sclerosis syndrome; Lymphangiomyomatosis
|Disease=Tuberous sclerosis 2; Tuberous sclerosis syndrome; Lymphangiomyomatosis
|CLNACC=RCV000013201.22; RCV000043065.2; RCV000055436.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1860707:613254:805; NBK1220:C0041341:191100:7199000; C0751674:606690:538:73017001
}}

{{PMID Auto
|PMID=9302281
|Title=The GAP-related domain of tuberin, the product of the TSC2 gene, is a target for missense mutations in tuberous sclerosis.
}}

{{PMID Auto
|PMID=10533067
|Title=Analysis of both TSC1 and TSC2 for germline mutations in 126 unrelated patients with tuberous sclerosis.
}}

{{PMID Auto
|PMID=10570911
|Title=Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complex.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}