{{Rsnum
|rsid=104894048
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SHH
|position=155803019
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SHH
}}{{omim
|id=600725
|rsnum=104894048
|variant=0012
}}{{ClinVar
|rsid=104894048
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=155595713
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SHH:6469
|GENE_NAME=SHH
|GENE_ID=6469
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.155595713G>C
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1530; 600725.0012
|CLNSIG=5
|CLNCUI=C1840529
|CLNDBN=Holoprosencephaly 3
|Disease=Holoprosencephaly 3
|CLNACC=RCV000009438.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1840529:142945:2162
}}