{{Rsnum
|rsid = 28936381
|Gene = GFI1
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=A
|MissenseAllele=G
|Chromosome=1
|position=92476153
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GFI1
}}{{omim
|desc=NEUTROPENIA, CONGENITAL, AUTOSOMAL DOMINANT 2
|id=600871
|rsnum=28936381
|variant=0001
}}{{ClinVar
|rsid=28936381
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=92476153
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=GFI1:2672
|GENE_NAME=GFI1
|GENE_ID=2672
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.92476153T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_005263.3:c.1145A>G; 600871.0001
|CLNSIG=5
|CLNCUI=C2751288
|CLNDBN=Severe congenital neutropenia 2, autosomal dominant
|Disease=Severe congenital neutropenia 2
|CLNACC=RCV000009278.1
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2751288:613107:ORPHA486
}}