{{Rsnum
|rsid=137854083
|Chromosome=16
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=TSC2
|position=2085302
|Gene_s=TSC2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNACC=RCV000013200.22; RCV000042568.2
|CLNALLE=1
|CLNDBN=Tuberous sclerosis 2; Tuberous sclerosis syndrome
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C1860707:613254:805; NBK1220:C0041341:191100:7199000
|CLNHGVS=NC_000016.9:g.2135303delC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant; Tuberous sclerosis database (TSC2)
|CLNSRCID=191092.0002; TSC2_00011
|Disease=Tuberous sclerosis 2; Tuberous sclerosis syndrome
|FwdREF=C
|GENEINFO=TSC2:7249
|GENE_ID=7249
|GENE_NAME=TSC2
|REF=TC
|RSPOS=2135301
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD
|VC=DIV
|VP=0x050268000000000002100200
|WGT=0
|dbSNPBuildID=133
|rsid=137854083
}}{{PMID Auto
|PMID=8634701
|Title=Mutation analysis of the TSC2 gene in an African-American family.
}}