{{Rsnum
|rsid=199476092
|Gene=PTCH1
|Chromosome=9
|position=95467197
|Orientation=minus
|GMAF=0.0009183
|Gene_s=PTCH1,RPL7L1P3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|rsid=199476092
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=98229479
|CHROM=9
|GMAF=0.0009
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050060000000000016110100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.98229479T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601309.0013
|CLNSIG=5
|CLNCUI=C1835820
|CLNDBN=Holoprosencephaly 7; not provided
|Disease=Holoprosencephaly 7; not provided
|CLNACC=RCV000008706.1; RCV000034565.1
|Tags=RV;PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9991; 0.0009183
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1835820:610828:2162
|COMMON=0
|GENEINFO=LOC100507346:100507346; PTCH1:5727
|GENE_ID=100507346; 5727
|GENE_NAME=LOC100507346; PTCH1
}}