{{Rsnum
|rsid=199476090
|Chromosome=9
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=PTCH1
|position=95479134
|Gene_s=PTCH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199476090
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=98241416
|CHROM=9
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.98241416G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601309.0003
|CLNSIG=5
|CLNCUI=C0004779
|CLNDBN=Gorlin syndrome
|Disease=Gorlin syndrome
|CLNACC=RCV000008696.1
|Tags=RV;PM;OTHERKG;LSD;OM
|GENEINFO=PTCH1:5727
|GENE_ID=5727
|GENE_NAME=PTCH1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT:SNOMED_CT
|CLNDSDBID=NBK1151:C0004779:109400:377:69408002:C0812437
}}