{{Rsnum
|rsid=137853230
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RECQL4
|position=144512033
|Gene_s=RECQL4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=603780
|variant=0010
|rsnum=137853230
}}{{ClinVar
|rsid=137853230
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=145737416
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=RECQL4:9401
|GENE_NAME=RECQL4
|GENE_ID=9401
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.145737416G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603780.0010
|CLNSIG=4
|CLNCUI=C1849453
|CLNDBN=Rapadilino syndrome
|Disease=Rapadilino syndrome
|CLNACC=RCV000049822.1
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1849453:266280:3021
}}{{PMID Auto
|PMID=12952869
|Title=Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases.
}}