{{Rsnum
|rsid=104894709
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=RFXANK
|position=19197545
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RFXANK
}}{{omim
|id=603200
|rsnum=104894709
|variant=0004
}}{{ClinVar
|rsid=104894709
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=19308354
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RFXANK:8625
|GENE_NAME=RFXANK
|GENE_ID=8625
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.19308354A>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000006979.1
|CLNDBN=BARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP B
|CLNDSDB=MedGen
|CLNDSDBID=C1859535
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=603200.0004
|Disease=BARE LYMPHOCYTE SYNDROME
}}