{{Rsnum
|rsid=121908952
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PAPSS2
|position=87727403
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAPSS2
}}{{omim
|id=603005
|rsnum=121908952
|variant=0003
}}{{ClinVar
|rsid=121908952
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=89487160
|CHROM=10
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=PAPSS2:9060
|GENE_NAME=PAPSS2
|GENE_ID=9060
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000010.10:g.89487160C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000007076.1
|CLNDBN=Spondyloepimetaphyseal dysplasia, pakistani type
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2748515:612847:93282
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603005.0003
|Disease=Spondyloepimetaphyseal dysplasia
}}