{{Rsnum
|rsid=45517148
|Chromosome=16
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=TSC2
|position=2060790
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TSC2
}}{{omim
|id=191092
|rsnum=45517148
|variant=0010
}}

{{ClinVar
|rsid=45517148
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=2110791
|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.2110791G>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=PM;PMC;GNO;OTHERKG;LSD;OM
|CLNACC=RCV000013209.2; RCV000042986.2; RCV000055263.1
|CLNDBN=Lymphangioleiomyomatosis, somatic; Tuberous sclerosis syndrome; Lymphangiomyomatosis
|CLNSRC=OMIM Allelic Variant; Tuberous sclerosis database (TSC2)
|CLNSRCID=191092.0010; TSC2_00383
|Disease=Lymphangioleiomyomatosis; Tuberous sclerosis syndrome; Lymphangiomyomatosis
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT; MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1220:C0041341:191100:7199000; C0751674:606690:538:73017001
}}

{{PMID Auto
|PMID=10823953
|Title=Mutations in the tuberous sclerosis complex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosis.
|OA=1
}}

{{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
}}

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