{{Rsnum
|rsid=104894902
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NSDHL
|position=152865903
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NSDHL
}}{{omim
|id=300275
|rsnum=104894902
|variant=0003
}}{{ClinVar
|rsid=104894902
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=152034447
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NSDHL:50814
|GENE_NAME=NSDHL
|GENE_ID=50814
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.152034447C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300275.0003
|CLNSIG=5
|CLNCUI=C0265267
|CLNDBN=Child syndrome
|Disease=Child syndrome
|CLNACC=RCV000012181.10
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK51754:C0265267:308050:139:17608003
}}