{{Rsnum
|rsid=121912739
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NPR2
|position=35800427
|Gene_s=NPR2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=108961
|rsnum=121912739
|variant=0004
}}{{ClinVar
|rsid=121912739
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=35800424
|CHROM=9
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NPR2:4882
|GENE_NAME=NPR2
|GENE_ID=4882
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.35800424C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=108961.0004
|CLNSIG=5
|CLNCUI=C1864356
|CLNDBN=Acromesomelic dysplasia Maroteaux type
|Disease=Acromesomelic dysplasia Maroteaux type
|CLNACC=RCV000019365.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1864356:602875:40
}}