{{Rsnum
|rsid=137852605
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=LBR
|position=225422087
|Gene_s=LBR
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600024
|variant=0004
|rsnum=137852605
}}{{ClinVar
|rsid=137852605
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=225422087
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=LBR:3930
|GENE_NAME=LBR
|GENE_ID=3930
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.225422087G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_194442.2:c.356C>T; 600024.0004
|CLNSIG=5
|CLNCUI=C0030779
|CLNDBN=Pelger-HuÃ«t anomaly
|Disease=Pelger-HuÃ«t anomaly
|CLNACC=RCV000010138.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0030779:169400:85559002
}}