{{Rsnum
|rsid = 28937580
|Gene = NOG
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=17
|position=56594326
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NOG
}}{{omim
|desc=SYMPHALANGISM, PROXIMAL
|id=602991
|rsnum=28937580
|variant=0012
}}

{{omim
|id=602991
|rsnum=28937580
|variant=0017
}}

{{ClinVar
|rsid=28937580
|Reversed=0
|FwdREF=C
|FwdALT=G,T
|REF=C
|ALT=G,T
|RSPOS=54671687
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=NOG:9241
|GENE_NAME=NOG
|GENE_ID=9241
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000017.10:g.54671687C>G; NC_000017.10:g.54671687C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602991.0017; 602991.0012
|CLNCUI=C1969652,C1861385; C1969652; C1866656
|CLNDBN=Brachydactyly type B2; Cushing's symphalangism; Stapes ankylosis with broad thumb and toes
|Disease=Brachydactyly type B2; Cushing's symphalangism; Stapes ankylosis with broad thumb and toes
|CLNACC=RCV000007100.1; RCV000007093.2; RCV000007094.2; RCV000007095.2
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM; MedGen:OMIM:Orphanet
|CLNDSDBID=C1969652:611377; C1861385:185800:3250; C1866656:184460:140917
|CLNSIG=5
}}

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