{{Rsnum
|rsid=74315322
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=HAX1
|position=154275165
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HAX1
}}{{omim
|id=605998
|rsnum=74315322
|variant=0001
}}{{ClinVar
|rsid=74315322
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=154275165
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000605000002110100
|GENEINFO=HAX1:10456
|GENE_NAME=HAX1
|GENE_ID=10456
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.154275165C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_006118.3:c.568C>T; 605998.0001
|CLNSIG=5
|CLNCUI=C1853118
|CLNDBN=Severe congenital neutropenia 3, autosomal recessive
|Disease=Severe congenital neutropenia 3
|CLNACC=RCV000004913.1
|Tags=PM;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1853118:610738:ORPHA99749
}}