{{Rsnum
|rsid=104894881
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NHS
|position=17375872
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NHS
}}{{omim
|id=300457
|rsnum=104894881
|variant=0005
}}{{ClinVar
|rsid=104894881
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=17393995
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NHS:4810
|GENE_NAME=NHS
|GENE_ID=4810
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.17393995C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300457.0005
|CLNSIG=5
|CLNCUI=C0796085
|CLNDBN=Nance-Horan syndrome
|Disease=Nance-Horan syndrome
|CLNACC=RCV000011774.5
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0796085:302350:627:445257004
}}