{{Rsnum
|rsid=137853229
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RECQL4
|position=144513412
|Gene_s=RECQL4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=603780
|variant=0002
|rsnum=137853229
}}{{ClinVar
|rsid=137853229
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=145738796
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RECQL4:9401
|GENE_NAME=RECQL4
|GENE_ID=9401
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.145738796G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=603780.0002
|CLNSIG=5
|CLNCUI=C0032339
|CLNDBN=Rothmund-Thomson syndrome
|Disease=Rothmund-Thomson syndrome
|CLNACC=RCV000006435.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1237:C0032339:268400:2909:69093006
}}