{{Rsnum
|rsid=267607145
|Chromosome=12
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TRPV4
|position=109798820
|Gene_s=TRPV4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=A
|CHROM=12
|CLNACC=RCV000005294.1; RCV000005295.1
|CLNALLE=1
|CLNDBN=Charcot-Marie-Tooth disease type 2C; Scapuloperoneal spinal muscular atrophy
|CLNDSDB=GeneReviews:MedGen:OMIM; MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1285:C2079540:606071; C0751335:181405:230248006
|CLNHGVS=NC_000012.11:g.110236625G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605427.0010
|Disease=Charcot-Marie-Tooth disease type 2C; Scapuloperoneal spinal muscular atrophy
|FwdALT=T
|FwdREF=C
|GENEINFO=TRPV4:59341
|GENE_ID=59341
|GENE_NAME=TRPV4
|REF=G
|RSPOS=110236625
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607145
}}