{{Rsnum
|rsid=113994150
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TSEN34
|position=54695387
|Assembly=GRCh37.p2
|GenomeBuild=37.2
|dbSNPBuild=134
|Gene_s=MBOAT7,TSEN34
}}{{omim
|id=608754
|rsnum=113994150
|variant=0001
}}{{ClinVar
|rsid=113994150
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=54695387
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=MBOAT7:79143; TSEN34:79042
|GENE_NAME=MBOAT7; TSEN34
|GENE_ID=79143; 79042
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.54695387C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK9673; 608754.0001
|CLNSIG=5
|CLNCUI=C2676465; C2676465
|CLNDBN=Pontocerebellar hypoplasia type 2C
|Disease=Pontocerebellar hypoplasia type 2C
|CLNACC=RCV000002206.1
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK9673:C2676465:612390:2524
}}