{{Rsnum
|rsid=267607026
|Chromosome=21
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=RUNX1
|position=34880598
|Gene_s=RUNX1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=21
|CLNACC=RCV000015558.24
|CLNALLE=1
|CLNDBN=Familial platelet disorder with associated myeloid malignancy
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1832388:601399:71290
|CLNHGVS=NC_000021.8:g.36252895G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=151385.0010
|Disease=Familial platelet disorder with associated myeloid malignancy
|FwdALT=A
|FwdREF=C
|GENEINFO=RUNX1:861
|GENE_ID=861
|GENE_NAME=RUNX1
|REF=G
|RSPOS=36252895
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267607026
}}