{{Rsnum
|rsid=267607035
|Chromosome=4
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SEPSECS
|position=25152049
|Gene_s=SEPSECS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=4
|CLNACC=RCV000000437.1
|CLNALLE=1
|CLNDBN=Pontocerebellar hypoplasia type 2D
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3151140:613811:2524
|CLNHGVS=NC_000004.11:g.25153671C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613009.0002
|Disease=Pontocerebellar hypoplasia type 2D
|FwdALT=A
|FwdREF=G
|GENEINFO=SEPSECS:51091
|GENE_ID=51091
|GENE_NAME=SEPSECS
|REF=C
|RSPOS=25153671
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607035
}}