{{Rsnum
|rsid=121434397
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PTCH2
|position=44827617
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=PTCH2
}}{{omim
|id=603673
|rsnum=121434397
|variant=0003
}}{{ClinVar
|rsid=121434397
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=44827617
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=PTCH2:8643
|GENE_NAME=PTCH2
|GENE_ID=8643
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.44827617C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001166292.1:c.2156G>A; 603673.0003
|CLNSIG=5
|CLNCUI=C0004779
|CLNDBN=Gorlin syndrome
|Disease=Gorlin syndrome
|CLNACC=RCV000006522.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1151:C0004779:109400:ORPHA377:69408002
}}