{{Rsnum
|rsid=267607047
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=SHH
|position=155806513
|Gene_s=SHH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=7
|CLNACC=RCV000009447.2
|CLNALLE=1
|CLNDBN=Holoprosencephaly 3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1840529:142945:2162
|CLNHGVS=NC_000007.13:g.155599207G>T
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1530; 600725.0020
|Disease=Holoprosencephaly 3
|FwdALT=A
|FwdREF=C
|GENEINFO=SHH:6469
|GENE_ID=6469
|GENE_NAME=SHH
|REF=G
|RSPOS=155599207
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607047
}}