{{Rsnum
|rsid=137854449
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ELANE
|position=853338
|Gene_s=ELANE
|Assembly=GRCh37.p5
|GenomeBuild=37.3
|dbSNPBuild=135
}}{{omim
|id=130130
|variant=0007
|rsnum=137854449
}}{{ClinVar
|rsid=137854449
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=853338
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ELANE:1991
|GENE_NAME=ELANE
|GENE_ID=1991
|WGT=0
|VC=SNV
|CLNALLE=2
|CLNHGVS=NC_000019.9:g.853338G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=130130.0010
|CLNSIG=5
|CLNCUI=C1859966
|CLNDBN=Severe congenital neutropenia autosomal dominant
|Disease=Severe congenital neutropenia autosomal dominant
|CLNACC=RCV000018231.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1533:C1859966:202700:486
}}