{{Rsnum
|rsid=137853098
|Chromosome=13
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RFXAP
|position=36819520
|Gene_s=RFXAP
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=601861
|variant=0004
|rsnum=137853098
}}{{ClinVar
|rsid=137853098
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=37393657
|CHROM=13
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RFXAP:5994
|GENE_NAME=RFXAP
|GENE_ID=5994
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000013.10:g.37393657C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000008091.1
|CLNDBN=Bare Lymphocyte Syndrome, Type II, Complementation Group D
|CLNDSDB=MedGen
|CLNDSDBID=C1859537
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=601861.0004
|Disease=Bare Lymphocyte Syndrome
}}