{{Rsnum
|rsid=112292549
|Gene=TGM5
|Chromosome=15
|position=43260151
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene_s=TGM5
}}{{omim
|id=603805
|rsnum=112292549
|variant=0001
}}{{ClinVar
|rsid=112292549
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=43552349
|CHROM=15
|GMAF=0.0014
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000040016110100
|GENEINFO=TGM5:9333
|GENE_NAME=TGM5
|GENE_ID=9333
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.43552349C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603805.0001
|CLNSIG=5
|CLNCUI=C1853354
|CLNDBN=Peeling skin syndrome, acral type
|Disease=Peeling skin syndrome
|CLNACC=RCV000006411.1
|Tags=PM;S3D;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1853354:609796:263534
|COMMON=0
}}