{{Rsnum
|rsid=121908089
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=NHP2
|position=178149760
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=NHP2
}}{{omim
|id=606470
|rsnum=121908089
|variant=0001
}}{{ClinVar
|rsid=121908089
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=177576761
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=NHP2:55651
|GENE_NAME=NHP2
|GENE_ID=55651
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.177576761A>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK22301; 606470.0001
|CLNSIG=5
|CLNCUI=C3151441
|CLNDBN=Dyskeratosis congenita, autosomal recessive 2; Dyskeratosis congenita autosomal recessive
|Disease=Dyskeratosis congenita; Dyskeratosis congenita autosomal recessive
|CLNACC=RCV000004501.1; RCV000032277.1
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C3151441:613987:1775; NBK22301:C1857144:224230:1775
}}