{{Rsnum
|rsid=137853099
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RFX5
|position=151344444
|Gene_s=RFX5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=601863
|variant=0005
|rsnum=137853099
}}{{ClinVar
|rsid=137853099
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=151344444
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=RFX5:5993
|GENE_NAME=RFX5
|GENE_ID=5993
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.151344444C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000449.3:c.446G>A; 601863.0005
|CLNSIG=5
|CLNCUI=C1859538
|CLNDBN=Bare lymphocyte syndrome type 2, complementation group E
|Disease=Bare lymphocyte syndrome type 2
|CLNACC=RCV000008087.1
|Tags=RV;PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1859538
}}