{{Rsnum
|rsid=121909833
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GAA)
|geno3=(GAA;GAA)
|Gene=NSDHL
|position=152867580
|Gene_s=NSDHL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300275
|rsnum=121909833
|variant=0008
}}{{ClinVar
|rsid=121909833
|Reversed=0
|FwdREF=GAA
|FwdALT=
|REF=GGAA
|ALT=G
|RSPOS=152036120
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110200
|GENEINFO=NSDHL:50814
|GENE_NAME=NSDHL
|GENE_ID=50814
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.152036124_152036126delGAA
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK51754; 300275.0008
|CLNSIG=5
|CLNCUI=C3151781; C3151781
|CLNDBN=NSDHL-Related Disorders
|Disease=NSDHL-Related Disorders
|CLNACC=RCV000020430.10
|Tags=PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK51754:C3151781:300831:251383
}}