{{Rsnum
|rsid=104894053
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=SHH
|position=155806475
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SHH
}}{{omim
|id=600725
|rsnum=104894053
|variant=0019
}}{{ClinVar
|rsid=104894053
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=155599169
|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.155599169C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600725.0019
|CLNSIG=5
|CLNCUI=C1840529; C1840235
|CLNDBN=Holoprosencephaly 3; Single upper central incisor
|Disease=Holoprosencephaly 3; Single upper central incisor
|CLNACC=RCV000009445.1; RCV000009446.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1840529:142945:2162; C1840235:147250:280200
}}