{{Rsnum
|rsid=397515376
|Chromosome=7
|Orientation=minus
|geno1=(-;-)
|geno2=(-;GCGCCCTTC)
|geno3=(GCGCCCTTC;GCGCCCTTC)
|Gene=SHH
|position=155803149
|Gene_s=SHH
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=7
|CLNACC=RCV000009439.2
|CLNALLE=1
|CLNDBN=Holoprosencephaly 3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1840529:142945:2162
|CLNHGVS=NC_000007.13:g.155595843_155595851delGAAGGGCGC
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1530; 600725.0013
|Disease=Holoprosencephaly 3
|FwdREF=GCGCCCTTC
|GENEINFO=SHH:6469
|GENE_ID=6469
|GENE_NAME=SHH
|REF=GGAAGGGCGC
|RSPOS=155595842
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397515376
}}