{{Rsnum
|rsid=113994149
|Gene=TSEN2
|Chromosome=3
|position=12516627
|Orientation=plus
|GMAF=0.0009183
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=TSEN2
}}{{omim
|id=608753
|rsnum=113994149
|variant=0001
}}{{ClinVar
|rsid=113994149
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=12558126
|CHROM=3
|GMAF=0.0009
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000016110100
|GENEINFO=TSEN2:80746
|GENE_NAME=TSEN2
|GENE_ID=80746
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.12558126A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK9673; 608753.0001
|CLNSIG=5
|CLNCUI=C2676466; C2676466
|CLNDBN=Pontocerebellar hypoplasia type 2B
|Disease=Pontocerebellar hypoplasia type 2B
|CLNACC=RCV000002207.1
|Tags=PM;S3D;SLO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK9673:C2676466:612389:2524
|COMMON=1
}}