{{Rsnum
|rsid=199476093
|Chromosome=9
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=PTCH1
|position=95459764
|Gene_s=PTCH1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199476093
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=98222046
|CHROM=9
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.98222046A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601309.0015
|CLNSIG=5
|CLNCUI=C1835820
|CLNDBN=Holoprosencephaly 7
|Disease=Holoprosencephaly 7
|CLNACC=RCV000008708.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1835820:610828:2162
|GENEINFO=PTCH1:5727
|GENE_ID=5727
|GENE_NAME=PTCH1
}}