{{Rsnum
|rsid=104893624
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CXCR4
|position=136114928
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CXCR4
}}{{omim
|id=162643
|rsnum=104893624
|variant=0001
}}{{ClinVar
|rsid=104893624
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=136872498
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CXCR4:7852
|GENE_NAME=CXCR4
|GENE_ID=7852
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.136872498G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=162643.0001
|CLNSIG=5
|CLNCUI=C0472817
|CLNDBN=Warts, hypogammaglobulinemia, infections, and myelokathexis; Myelokathexis, isolated
|Disease=Warts; Myelokathexis
|CLNACC=RCV000015063.20; RCV000015064.24
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0472817:193670:51636:234571003
}}