{{Rsnum
|rsid=121918545
|Chromosome=14
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=TINF2
|position=24240636
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TINF2
}}{{omim
|id=604319
|rsnum=121918545
|variant=0003
}}{{ClinVar
|rsid=121918545
|Reversed=1
|FwdREF=C
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=24709842
|CHROM=14
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050160000000000002110100
|GENEINFO=TINF2:26277
|GENE_NAME=TINF2
|GENE_ID=26277
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000014.8:g.24709842G>A; NC_000014.8:g.24709842G>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK22301; 604319.0004; 604319.0003
|CLNSIG=5
|CLNCUI=C3151445
|CLNDBN=Dyskeratosis congenita, autosomal dominant, 3; Dyskeratosis congenita autosomal dominant
|Disease=Dyskeratosis congenita; Dyskeratosis congenita autosomal dominant
|CLNACC=RCV000005981.1; RCV000032169.1; RCV000005980.1; RCV000032168.1
|Tags=RV;PM;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C3151445:613990:1775; NBK22301:C1851970:127550:1775
}}