{{Rsnum
|rsid=193922415
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=WAS
|position=48683890
|Gene_s=WAS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922415
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=48542279
|CHROM=X
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050068000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.48542279C>T
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=5
|CLNDBN=Wiskott-Aldrich syndrome
|Disease=Wiskott-Aldrich syndrome
|Tags=PM;PMC;OTHERKG;LSD
|CLNACC=RCV000030595.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1178:C0043194:301000:906:36070007
|GENEINFO=WAS:7454
|GENE_ID=7454
|GENE_NAME=WAS
}}{{PMID Auto
|PMID=12969986
|Title=Clinical course of patients with WASP gene mutations.
}}

{{PMID Auto
|PMID=17400488
|Title=Detection of 28 novel mutations in the Wiskott-Aldrich syndrome and X-linked thrombocytopenia based on multiplex PCR.
}}

{{PMID Auto
|PMID=17703096
|Title=Clinical aspects and molecular analysis of Chinese patients with Wiskott-Aldrich syndrome in Taiwan.
}}

{{PMID Auto
|PMID=18162713
|Title=A familial case of Wiskott-Aldrich Syndrome with a hotspot mutation in exon 2 of the WAS Gene.
|OA=1
}}