{{Rsnum
|rsid=199473705
|Chromosome=17
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=TRPV3
|position=3518587
|Gene_s=TRPV3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199473705
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=3421881
|CHROM=17
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.3421881A>C
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|CLNACC=RCV000023613.1; RCV000059644.2
|CLNDBN=Palmoplantar keratoderma, mutilating, with periorificial keratotic plaques; not provided
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2609071:614594:659
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=607066.0003; VAR_067922
|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
}}