{{Rsnum
|rsid = 28933685
|Gene = NDP
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=X
|position=43958645
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NDP
}}{{omim
| id = 310600
| variant = 0009
| desc    = NORRIE DISEASE
| rsnum   = 28933685
}}
{{ neighbor
| rsid = 28933684
| distance = 8814
}}

{{omim
|id=300658
|rsnum=28933685
|variant=0009
}}

{{ClinVar
|rsid=28933685
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=43817891
|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.43817891T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300658.0009
|CLNSIG=5
|CLNCUI=C0266526
|CLNDBN=Atrophia bulborum hereditaria
|Disease=Atrophia bulborum hereditaria
|CLNACC=RCV000011433.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1331:C0266526:310600:649:15228007
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}