{{Rsnum
|rsid=104894049
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=SHH
|position=155806527
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SHH
}}{{omim
|id=600725
|rsnum=104894049
|variant=0014
}}{{ClinVar
|rsid=104894049
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=155599221
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=SHH:6469
|GENE_NAME=SHH
|GENE_ID=6469
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.155599221T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600725.0014
|CLNSIG=5
|CLNCUI=C1840235
|CLNDBN=Single upper central incisor
|Disease=Single upper central incisor
|CLNACC=RCV000009440.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1840235:147250:280200
}}