{{Rsnum
|rsid=104894212
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=DHCR7
|position=71438966
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DHCR7
}}{{omim
|id=602858
|rsnum=104894212
|variant=0008
}}{{ClinVar
|rsid=104894212
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=71150012
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=DHCR7:1717
|GENE_NAME=DHCR7
|GENE_ID=1717
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.71150012C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602858.0008
|CLNSIG=5
|CLNCUI=C0175694
|CLNDBN=Smith-Lemli-Opitz syndrome
|Disease=Smith-Lemli-Opitz syndrome
|CLNACC=RCV000007184.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1143:C0175694:270400:818:43929004
}}