{{Rsnum
|rsid = 28936675
|Gene = SHH
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=7
|position=155812032
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SHH
}}{{omim
|desc=HOLOPROSENCEPHALY 3
|id=600725
|rsnum=28936675
|variant=0001
}}

{{ClinVar
|rsid=28936675
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=155604726
|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.155604726C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1530; 600725.0001
|CLNSIG=5
|CLNCUI=C1840529
|CLNDBN=Holoprosencephaly 3
|Disease=Holoprosencephaly 3
|CLNACC=RCV000009427.2
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1530:C1840529:142945:2162
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}