{{Rsnum
|rsid=121908951
|Chromosome=10
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=PAPSS2
|position=87709311
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PAPSS2
}}{{omim
|id=603005
|rsnum=121908951
|variant=0002
}}{{ClinVar
|rsid=121908951
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=89469068
|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.89469068C>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000007075.1
|CLNDBN=Spondyloepimetaphyseal dysplasia, pakistani type
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2748515:612847:93282
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603005.0002
|Disease=Spondyloepimetaphyseal dysplasia
}}