{{Rsnum
|rsid=121912637
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TRPV4
|position=109784378
|Gene_s=TRPV4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=605427
|rsnum=121912637
|variant=0007
}}{{ClinVar
|rsid=121912637
|Reversed=1
|FwdREF=C
|FwdALT=G,T
|REF=G
|ALT=A,C
|RSPOS=110222183
|CHROM=12
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TRPV4:59341
|GENE_NAME=TRPV4
|GENE_ID=59341
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000012.11:g.110222183G>A; NC_000012.11:g.110222183G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605427.0007; 605427.0015
|CLNSIG=5
|CLNCUI=C0265281; CN033487
|CLNDBN=Metatrophic dysplasia; Spondyloepiphyseal dysplasia Maroteaux type
|Disease=Metatrophic dysplasia; Spondyloepiphyseal dysplasia Maroteaux type
|CLNACC=RCV000005287.1; RCV000005288.1; RCV000005300.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT; MedGen:OMIM:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265281:156530:2635:22764001; C3159322:184095:613678:263482:389165004
}}