{{Rsnum
|rsid = 28938174
|Gene = DHCR7
|geno1 = (A;A)
|geno2 = (A;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=T
|Chromosome=11
|position=71442319
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=DHCR7
}}{{omim
|desc=SMITH-LEMLI-OPITZ SYNDROME
|id=602858
|rsnum=28938174
|variant=0005
}}

{{ClinVar
|rsid=28938174
|Reversed=1
|FwdREF=A
|FwdALT=T
|REF=T
|ALT=A
|RSPOS=71153365
|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.71153365T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602858.0005
|CLNSIG=5
|CLNCUI=C0175694
|CLNDBN=Smith-Lemli-Opitz syndrome
|Disease=Smith-Lemli-Opitz syndrome
|CLNACC=RCV000007182.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1143:C0175694:270400:818:43929004
}}

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