{{Rsnum
|rsid=104894877
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NDP
|position=43949913
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NDP
}}{{omim
|id=300658
|rsnum=104894877
|variant=0018
}}{{ClinVar
|rsid=104894877
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=43809159
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NDP:4693
|GENE_NAME=NDP
|GENE_ID=4693
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.43809159G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300658.0018
|CLNSIG=5
|CLNCUI=C0266526
|CLNDBN=Atrophia bulborum hereditaria
|Disease=Atrophia bulborum hereditaria
|CLNACC=RCV000011442.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1331:C0266526:310600:649:15228007
}}