{{Rsnum
|rsid=132630274
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WAS
|position=48688331
|Gene_s=WAS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300392
|variant=0012
|rsnum=132630274
}}{{ClinVar
|rsid=132630274
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=48546720
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=WAS:7454
|GENE_NAME=WAS
|GENE_ID=7454
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.48546720T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300392.0012
|CLNSIG=5
|CLNCUI=C1845987
|CLNDBN=Severe congenital neutropenia X-linked
|Disease=Severe congenital neutropenia X-linked
|CLNACC=RCV000011874.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1178:C1845987:300299:86788
}}