{{Rsnum
|rsid=45517259
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TSC2
|position=2076142
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TSC2
}}{{omim
|id=191092
|rsnum=45517259
|variant=0013
}}

{{ClinVar
|rsid=45517259
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=2126143
|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
|CLNHGVS=NC_000016.9:g.2126143G>A
|CLNSRC=OMIM Allelic Variant; Tuberous sclerosis database (TSC2)
|CLNORIGIN=1
|CLNSRCID=191092.0013; TSC2_00134
|CLNSIG=5
|CLNCUI=C1860707
|CLNDBN=Tuberous sclerosis 2; Tuberous sclerosis syndrome
|Disease=Tuberous sclerosis 2; Tuberous sclerosis syndrome
|CLNACC=RCV000013212.15; RCV000042875.2
|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=157987
|Title=Disablement in society: towards an integrated perspective.
}}

{{PMID Auto
|PMID=9829910
|Title=Exon scanning of the entire TSC2 gene for germline mutations in 40 unrelated patients with tuberous sclerosis.
}}

{{PMID Auto
|PMID=11112665
|Title=Mutational analysis in a cohort of 224 tuberous sclerosis patients indicates increased severity of TSC2, compared with TSC1, disease in multiple organs.
|OA=1
}}

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

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | HumanOmni1Quad}}