{{Rsnum
|rsid = 28933690
|Gene = XK
|Orientation=minus
|ReferenceAllele=T
|MissenseAllele=C
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Chromosome=X
|position=37728007
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=XK
}}{{omim
|desc=MCLEOD SYNDROME
|id=314850
|rsnum=28933690
|variant=0005
}}

{{ClinVar
|rsid=28933690
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=37587260
|CHROM=X
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050060000000000402110100
|GENEINFO=XK:7504
|GENE_NAME=XK
|GENE_ID=7504
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.37587260T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=314850.0005
|CLNSIG=5
|CLNCUI=CN069344
|CLNDBN=McLeod neuroacanthocytosis syndrome
|Disease=McLeod neuroacanthocytosis syndrome
|CLNACC=RCV000010422.1
|Tags=PM;HD;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1354:CN069344:300842:59306
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}