{{Rsnum
|rsid=132630268
|Chromosome=X
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=WAS
|position=48684407
|Gene_s=WAS
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300392
|variant=0002
|rsnum=132630268
}}
{{omim
|id=300392
|variant=0003
|rsnum=132630268
}}{{ClinVar
|rsid=132630268
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=48542796
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=WAS:7454
|GENE_NAME=WAS
|GENE_ID=7454
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.48542796G>A; NC_000023.10:g.48542796G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300392.0003; 300392.0002
|CLNSIG=5
|CLNCUI=C0043194
|CLNDBN=Wiskott-Aldrich syndrome
|Disease=Wiskott-Aldrich syndrome
|CLNACC=RCV000011864.4; RCV000011863.16
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1178:C0043194:301000:906:36070007
}}