{{Rsnum
|rsid=121434412
|Chromosome=2
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=AGPS
|position=177461948
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AGPS
}}{{omim
|id=603051
|rsnum=121434412
|variant=0002
}}{{ClinVar
|rsid=121434412
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=178326676
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=AGPS:8540
|GENE_NAME=AGPS
|GENE_ID=8540
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.178326676C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603051.0002
|CLNSIG=5
|CLNCUI=C1838612
|CLNDBN=Rhizomelic chondrodysplasia punctata type 3
|Disease=Rhizomelic chondrodysplasia punctata type 3
|CLNACC=RCV000007025.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1838612:600121:177
}}