{{Rsnum
|rsid=45516293
|Chromosome=16
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=TSC2
|position=2084965
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TSC2
}}{{omim
|id=191092
|rsnum=45516293
|variant=0011
}}
{{omim
|id=191100
|rsnum=45516293
}}

{{ClinVar
|rsid=45516293
|Reversed=0
|FwdREF=A
|FwdALT=C
|REF=A
|ALT=C
|RSPOS=2134966
|CHROM=16
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050068000000000102110100
|GENEINFO=TSC2:7249
|GENE_NAME=TSC2
|GENE_ID=7249
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.2134966A>C
|CLNSRC=OMIM Allelic Variant; Tuberous sclerosis database (TSC2)
|CLNORIGIN=1
|CLNSRCID=191092.0011; TSC2_00747
|CLNSIG=5
|CLNCUI=C1860707
|CLNDBN=Tuberous sclerosis 2; Tuberous sclerosis syndrome
|Disease=Tuberous sclerosis 2; Tuberous sclerosis syndrome
|CLNACC=RCV000013210.23; RCV000043266.2
|Tags=PM;PMC;GNO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C1860707:613254:805; NBK1220:C0041341:191100:7199000
}}

{{PMID Auto
|PMID=11403047
|Title=A novel missense mutation in the GTPase activating protein homology region of TSC2 in two large families with tuberous sclerosis complex.
|OA=1
}}

{{PMID Auto
|PMID=17304050
|Title=Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States.
}}

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