{{Rsnum
|rsid=45517258
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TSC2
|position=2076141
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TSC2
}}{{omim
|id=191092
|rsnum=45517258
|variant=0014
}}
{{omim
|id=191092
|rsnum=45517258
|variant=0015
}}

{{ClinVar
|rsid=45517258
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=2126142
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050068000000000502110100
|GENEINFO=TSC2:7249
|GENE_NAME=TSC2
|GENE_ID=7249
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000016.9:g.2126142C>G; NC_000016.9:g.2126142C>T
|CLNSRC=OMIM Allelic Variant; Tuberous sclerosis database (TSC2)
|CLNORIGIN=1
|CLNSRCID=191092.0015; TSC2_00259; 191092.0014; TSC2_00110
|CLNSIG=5
|CLNCUI=C1860707
|CLNDBN=Tuberous sclerosis 2; Tuberous sclerosis syndrome
|Disease=Tuberous sclerosis 2; Tuberous sclerosis syndrome
|CLNACC=RCV000013214.23; RCV000042482.2; RCV000013213.21; RCV000042962.2
|Tags=PM;PMC;HD;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C1860707:613254:805; NBK1220:C0041341:191100:7199000
}}

{{PMID Auto
|PMID=12015165
|Title=Novel TSC1 and TSC2 mutations in Japanese patients with tuberous sclerosis complex.
}}

{{PMID Auto
|PMID=15798
|Title=Fengnan County's heroic barefoot doctors.
}}

{{PMID Auto
|PMID=10607950
|Title=Analysis of all exons of TSC1 and TSC2 genes for germline mutations in Japanese patients with tuberous sclerosis: report of 10 mutations.
}}

{{PMID Auto
|PMID=14641237
|Title=A 34 bp deletion within TSC2 is a rare polymorphism, not a pathogenic mutation.
}}

{{PMID Auto
|PMID=15798777
|Title=Mutational analysis of the TSC1 and TSC2 genes in a diagnostic setting: genotype--phenotype correlations and comparison of diagnostic DNA techniques in Tuberous Sclerosis Complex.
}}

{{PMID Auto
|PMID=17120248
|Title=Unusually mild tuberous sclerosis phenotype is associated with TSC2 R905Q mutation.
}}

{{on chip | HumanOmni1Quad}}