{{Rsnum
|rsid=199473704
|Chromosome=17
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TRPV3
|position=3524224
|Gene_s=TRPV3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199473704
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=3427518
|CHROM=17
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000017.10:g.3427518C>A; NC_000017.10:g.3427518C>T
|CLNORIGIN=1
|CLNSRCID=
607066.0002; VAR_067920; 607066.0001; VAR_067921
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000023612.1; RCV000059643.2; RCV000023611.1; RCV000059642.2
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|CLNDBN=Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2609071:614594:659
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|Disease=Palmoplantar keratoderma; not provided
|GENEINFO=TRPV3:162514
|GENE_ID=162514
|GENE_NAME=TRPV3
}}{{PMID Auto
|PMID=22405088
|Title=Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome.
|OA=1
}}