{{Rsnum
|rsid=137852219
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PORCN
|position=48511380
|Gene_s=PORCN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300651
|variant=0004
|rsnum=137852219
}}{{ClinVar
|rsid=137852219
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=48369768
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=PORCN:64840
|GENE_NAME=PORCN
|GENE_ID=64840
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.48369768G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300651.0004
|CLNSIG=5
|CLNCUI=C0016395
|CLNDBN=Focal dermal hypoplasia
|Disease=Focal dermal hypoplasia
|CLNACC=RCV000011449.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1543:C0016395:305600:2092
}}